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Octanoyl chloride → S-{3-[(Dimethoxymethyl)silyl]propyl} octanethioate

HRID 1020517
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반응식

HRID 1020517 반응식
C(N(CC)CC)C.[C:8](Cl)(=[O:16])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[SH:18][CH2:19][CH2:20][CH2:21][SiH2:22][CH:23]([O:26][CH3:27])[O:24][CH3:25]>C1(C)C=CC=CC=1>[C:8]([S:18][CH2:19][CH2:20][CH2:21][SiH2:22][CH:23]([O:26][CH3:27])[O:24][CH3:25])(=[O:16])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8124Octanoyl chlorideHCID 8471TriethylamineHCID 169231HCID 169231, 화합물

생성물 1

HCID 71417114S-{3-[(Dimethoxymethyl)silyl]propyl} octanethioate수율 95%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

In a four-necked flask of 1 L, 18.0 g of 3-mercaptopropyl dimethoxymethyl silane and 11.1 g of triethylamine are dissolved in 300 mL of toluene under a nitrogen atmosphere. To this solution is added 16.2 g of octanoic acid chloride dropwise over 30 minutes, which is stirred for 2 hours. Thereafter, the precipitates are filtered off and the solvent is removed by a rotary evaporator at 20 hPa/40° C. to obtain 29.0 g of 3-octanoylthio-propyl dimethoxymethyl silane.

후처리

  1. filtrationThereafter, the precipitates are filtered off
  2. customthe solvent is removed by a rotary evaporator at 20 hPa/40° C.

출처 및 근거

ORD 기록
ord-4b5bc8b5a7484163940cbf305dd5de7e
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716375B2

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