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Sodium Hydroxide → 2-Cyanomethyl-3-octadecylcarbamoyloxypropanol

HRID 728502
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인쇄 미리보기

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HRID 728502 반응식
C([O:9][CH2:10][CH:11]([CH2:35][C:36]#[N:37])[CH2:12][O:13][C:14](=[O:34])[NH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])(=O)C1C=CC=CC=1.[OH-].[Na+].C(CC(COCCCCCCCCCCCCCCCC)CO)#N>CO.O1CCCC1>[C:36]([CH2:35][CH:11]([CH2:12][O:13][C:14](=[O:34])[NH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[CH2:10][OH:9])#[N:37]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 14798Sodium HydroxideHCID 148349942-Cyanomethyl-3-hexadecyloxypropanolHCID 541175562-Cyanomethyl-3-octadecylcarbamoyloxypropyl benzoate

생성물 1

HCID 148349952-Cyanomethyl-3-octadecylcarbamoyloxypropanol수율 81.3%

시약·촉매·용매 2

HCID 887Methanol용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

A mixture of 1.49 g (2.96 mM) of 2-cyanomethyl-3-n-octadecylcarbamoyloxypropyl benzoate n5', 1.66 ml (3.32 mM) of 2N aqueous sodium hydroxide in 15 ml of methanol and 15 ml of tetrahydrofuran is allowed to react by the same procedure as described in (137) and 966 mg (76.8% yield) of the titled compound Vn2 is obtained.

후처리

  1. customto react by the same procedure

출처 및 근거

ORD 기록
ord-9c494ecd3ab04e5282f6ce1367fbd713
출처 데이터셋
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05047540

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