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CAS No. : | 77897-23-5 | MDL No. : | MFCD11519115 |
Formula : | C11H15NO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | LSXCLMMIDIVSFG-NSHDSACASA-N |
M.W : | 177.24 | Pubchem ID : | 10487535 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362 | UN#: | N/A |
Hazard Statements: | H315-H319 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
50%; 43% | In dichloromethane; for 48h; | General procedure: Example 43: Kinetic Resolution of Racemic 3-Benzyl- morpholine with Polymer Supported Reagent (R,S) -10Racemic 3-benzylmorpholine (79.0 mg, 0.45 mmol, 1.00 equiv) , in CH2C12 (2 ml) was resolved according to the general procedure of Example 31 by treatment with the resin supported reagent 10 (Example 41; 300 mg, ~1.00 mmol/g, -0.65 - 0.70 equiv) for 48 h. The solution from the polymer support wash was concentrated under reduced pressure and the amide product and unreacted amine were separated by column chromatography (CH2Cl2: eOH 95:5 for amide) ( CH2C12 : MeOH 1:1 for amine) .Recovered amine 40 mg (50% yield, er = 87:13); acylated product 68 mg (43% yield, er = 92:8) .Calculated conversion c = 47%, s = 25.(S)-l-(3- Benzylmorpholino) -3- (2- nitrophenyl)propan-1 -one (amide product) [a] 23D (c = 0.75, CHC13) -14.4 ( er = 92:8); H NMR (400 MHz, CDCl3) δ 7.90 (m, 1H) , 7.55 (m, 1H) , 7.45- 7.30 (m, 2H), 7.30-7.10 (m, 5H) , 6.75 (m, 0.1H), 4.65 (m, 0.4H), 4.42 (apparent dd, J = 13.8, 2.6, 0.5H), 3.95 (m, 1H), 3.75 (m, 1.5H), 3.60-3.30 (m, 2.4H), 3.20-3.00 (m, 2.8H), 3.00-2.90 (m, 1H) , 2.85-2.65 (m, 1.5H), 2.60-2.50 (m, 1H), 2.0 (m, 0.6H), 1.80 (m, 0.2H);13C NMR (100 MHz, CDC13) δ 175.6, 170.8, 170.5, 149.3, 133.1, 132.8, 129.6, 129.3, 128.8, 128.5, 127.4, 126.9, 124.8, 124.7, 114.3, 68.9, 67.4, 67.2, 66.7, 55.5, 50.5, 41.8, 37.2, 35.8, 34.7, 34.4, 34.2, 33.2, 29.1, 28.8, 28.2;HRMS (ESI) calculated for [C20H22N2O,jNa ] + m/z = 377.1472; found m/z = 377.1465;IR (u/cnf1, neat) 2923, 2858, 1643, 1523, 1495, 1426, 1348, 1119;SFC column: Daicel Chiralpak ADH (4.6 χ 250 mm); gradient: 5% iPrOH in C02 to 50% iPrOH in C02 over 10 min; flow: 3.0 ml/min; detection: 254 nm. Retention time: tR = 7.3 min (minor), 7.6 min (major) .(R) -3-Benzylmophol ine (recovered amine)[ aj D (c = 0.75, CHCI3) : +11.7 (er = 92:8); Amine was converted into an amide by using 3 phenylpropanoyl chloride and Et3N to determine er by SFC;SFC: column: Daicel Chiralpak OJH (4.6 χ 250 mm) gradient: 5% iPrOH in C02 to 50% iPrOH in C02 over 10 min flow: 3.0 ml/min; detection: 254 nm. Retention time tR = 5.8 min (major), 6.4 min (minor) . |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
66%; 31% | With 2-(2,4,6-trimethyl-phenyl)-2,5,6,7-tetrahydro-pyrrolo[2,1-c] [1,2,4]triazol-4-ylium perchlorate; (4aR,9aS)-6-bromo-4-hydroxy-4,4a,9,9a-tetrahydroindeno[2,1-b][1,4]oxazin-3(2H)-one; potassium carbonate; In tetrahydrofuran; at 23℃; for 36h; | Example 52: Procedure for Kinetic Resolution with α'- HydroxydienoneHydroxamic acid co-catalyst 1 (Example 18; 7.1 mg, 25 pmol, 0.05 equiv) , triazolium salt (16.4 mg, 50 μιηο, 0.10 equiv) , a ' -hydroxydienone (75.6 mg, 0.35 mmol, 0.70 equiv), K2C03 (13.8 mg, 0.1 mmol, 0.20 equiv) and 3- benzylmorpholine (88.6 mg, 0.50 mmol, 1.00 equiv) were dissolved in THF (2.5 ml, 0.20 M) and the reaction mixture was stirred at 23 C for 36 hours.Ethyl acetate (2.5 ml) was added and the organic phase was washed with 1 M HC1 (3 > 2 ml) and the organic layer was dried (Na2S04) and concentrated in vacuo to give the crude amide product, which was purified by column chromatography. The combined acidic aqueous phases were basified with solid K2C03, extracted with CH2C12 (3 * 5 ml) , dried (Na2S04) and concentrated in vacuo to give the recovered amine.Recovered amine: 59 mg (66%, er = 70:30); acylated product: 52 mg (31%, er = 93:7) .Calculated conversion: 32%; s = 20 |
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