天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List N-Boc-(ethylamino)acetaldehyde
315718-06-0

N-Boc-(ethylamino)acetaldehyde synthesis

3synthesis methods
-

Yield:-

Reaction Conditions:

with triethylamine in methanol;dichloromethane;water;dimethyl sulfoxide;

Steps:

29.B Step B

Step B 2-(N-Tert-butyloxycarbonyl-N-ethyl)aminoacetaldehyde To a mixture of oxalyl chloride (3.4 ml of 2M solution in CH2Cl2, 6.87 mmol) in CH2Cl2 (10 ml) at -78° C. was added a solution of DMSO (0.86 ml, 12.14 mmol) in CH2Cl2 (5 ml) slowly. The mixture was stirred at -78° C. for 20 min. To this was added a solution of 2-(N-Tert-butyloxycarbonyl-N-ethyl)aminoethanol (1.0 g, 5.28 mmol) in CH2Cl2 (5 ml) slowly. The reaction mixture was then stirred at -78° C. for 2 h followed by addition of triethylamine (3.7 ml, 26.4 mmol). The mixture was stirred again at -78° C. for 10 min, at 0° C. for 30 min. A mixture of methanol (1 ml) and water (8 ml) was added to the reaction; the mixture was separated. The aqueous layer was extracted with methylene chloride (3*60 ml). The combined organic layer was washed with saturated sodium bicarbonate, water, brine and dried over magnesium sulfate. Removal of the solvent provided the title compound, which was used directly for next step.

References:

US6316444,2001,B1

N-Boc-(ethylamino)acetaldehyde Related Search: