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1-[3-(tert-Butyldimethylsilyloxymethyl)phenyl]-3-mesitylthiourea → 1-(3-Hydroxymethylphenyl)-3-mesitylthiourea

HRID 2235522
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인쇄 미리보기

반응식

HRID 2235522 반응식
[Si]([O:8][CH2:9][C:10]1[CH:11]=[C:12]([NH:16][C:17]([NH:19][C:20]2[C:25]([CH3:26])=[CH:24][C:23]([CH3:27])=[CH:22][C:21]=2[CH3:28])=[S:18])[CH:13]=[CH:14][CH:15]=1)(C(C)(C)C)(C)C>C(O)C.Cl.O>[OH:8][CH2:9][C:10]1[CH:11]=[C:12]([NH:16][C:17]([NH:19][C:20]2[C:25]([CH3:26])=[CH:24][C:23]([CH3:27])=[CH:22][C:21]=2[CH3:28])=[S:18])[CH:13]=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 875051471-[3-(tert-Butyldimethylsilyloxymethyl)phenyl]-3-mesitylthiourea

생성물 1

HCID 860491161-(3-Hydroxymethylphenyl)-3-mesitylthiourea수율 86.3%

시약·촉매·용매 3

HCID 313Hydrochloric Acid촉매HCID 702Ethanol용매HCID 962Water용매

실험 절차

To 0.56 g (0.1.4 mmol) of 1-[3-(tert-butyldimethylsilyloxymethyl)phenyl]-3-mesitylthiourea in 10 mL of ethanol was added 10 drops of concentrated hydrochloric acid. After 30 min, the reaction was diluted with water and the precipitate that formed was collected to give 0.35 g (86%) of the title compound as a white powder.

후처리

  1. customthe precipitate that formed
  2. customwas collected

출처 및 근거

ORD 기록
ord-627e7054d6c94f209827bcfc7adffd8c
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714009B2

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