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106429-67-8

(1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL synthesis

7synthesis methods
-

Yield:106429-67-8 81%

Reaction Conditions:

with lithium aluminium tetrahydride in tetrahydrofuran at 20; for 4 h;

Steps:



LiAlH4 (0.316 g, 7.90 mmol) and THF (15 mL). Methyl lH-benzo[d][l,2,3]triazole- 5-carboxylate (1.0 g, 5.64 mmol) was then added portion-wise over lOmin at room temperature and reaction allowed to stir for 4 hours at which time the reaction was quenched with EtOAc (5 mL), and the mixture poured into ice-water. The mixture was acidified to pH = 3 with 10% H2SO4 and extracted 4X with EtOAc. The combined organics were washed with brine, dried (MgSO4) and the solvent removed. The resulting brown solid was boiled in Et2O and the solids filtered and dried to give the title compound as a light brown solid (678 mg, 81 %). 1H NMR (400 MHz, CD3OD) δ 7.85 (m, 2H), 7.47 (d, J= 8.4 Hz, IH), 4.79 (s, 2H); MS ESI 150.0 [M + H]+, calcd for [C7H7N3O + H]+ 150.16.

References:

WO2009/79767,2009,A1 Location in patent:Page/Page column 83

491612-10-3 Synthesis
2-(1H-1,2,3-benzotriazol-5-yl)acetic acid

491612-10-3
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(1H-BENZO[D][1,2,3]TRIAZOL-5-YL)METHANOL

106429-67-8
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