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Trityl chloride → 3-[(Triphenylmethyl)sulfanyl]propanoic acid

HRID 444609
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인쇄 미리보기

반응식

HRID 444609 반응식
[CH2:1]([C:4]([OH:6])=[O:5])[CH2:2][SH:3].[C:7]1([C:13](Cl)([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(Cl)Cl>[C:13]([S:3][CH2:2][CH2:1][C:4]([OH:6])=[O:5])([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6456Trityl chlorideHCID 65143-Mercaptopropionic Acid

생성물 1

HCID 2627673-[(Triphenylmethyl)sulfanyl]propanoic acid수율 95.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Mercaptopropionic acid 12 (3.14 g) was dissolved in 50 ml of methylene chloride. Triphenylmethylchloride 13 (8.36 g) was added to that, and 19-hour reactions were carried out at room temperature. The precipitate generated through the reactions was gathered by filtration, and the solid components obtained here were dried under reduced pressure, to form 9.86 g of 3-(tritylthio)propionic acid 14, which is a white solid.

후처리

  1. customwere carried out at room temperature
  2. filtrationwas gathered by filtration
  3. customthe solid components obtained here
  4. customwere dried under reduced pressure

출처 및 근거

ORD 기록
ord-cc51c2cc70eb48d5b5288f27eea55aa0
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08475685B2

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