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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethyl Sulfoxide → 3-Methyl-5-(trifluoromethyl)benzaldehyde

HRID 1194745
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인쇄 미리보기

반응식

HRID 1194745 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[F:11][C:12]([F:23])([F:22])[C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([CH3:21])[CH:20]=1)[CH2:16][OH:17].C(N(CC)CC)C>C(Cl)Cl>[F:11][C:12]([F:22])([F:23])[C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([CH3:21])[CH:20]=1)[CH:16]=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 2775612(3-Methyl-5-(trifluoromethyl)phenyl)methanol

생성물 1

HCID 230362293-Methyl-5-(trifluoromethyl)benzaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

A solution fo oxalyl chloride (2.8 ml) in 20 ml of CH2Cl2 is treated with a solution of dimethyl sulfoxide (DMSO)(5.0 ml) in 15 ml of CH2Cl2 at -60° C. as in Example 11 To this mixture is added the 3-trifluoromethyl-5-methylbenzyl alcohol (5.4 g) in CH2Cl2 (20 ml) followed by 20 ml of triethlyamine. Appropriate reaction conditions and work-up as in Example 11 afforded 3-trifluoro- methyl-5-methylbenzaldehyde.

후처리

  1. customAppropriate reaction conditions

출처 및 근거

ORD 기록
ord-c20a28d229b84864ba030f1b779000e1
출처 데이터셋
uspto-grants-1989_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04816469

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