홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Oxalyl chloride → (2-Bromo-5-methoxy-4-methyl-phenyl)-acetic acid chloride

HRID 1691781
노트
인쇄 미리보기

반응식

HRID 1691781 반응식
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([O:9][CH3:10])=[CH:4][C:3]=1[CH2:11][C:12]([OH:14])=O.C(Cl)(=O)C([Cl:18])=O>ClCCl.CN(C=O)C>[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([O:9][CH3:10])=[CH:4][C:3]=1[CH2:11][C:12]([Cl:18])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 291672(2-Bromo-5-methoxy-4-methylphenyl)acetic acid

생성물 1

HCID 59377714(2-Bromo-5-methoxy-4-methyl-phenyl)-acetic acid chloride

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of (2-bromo-5-methoxy-4-methyl-phenyl)-acetic acid (149.4 mg) in dichloromethane (1.8 mL) was added oxalyl chloride (0.055 mL) followed by DMF (1 drop) uder argon. Mixture was stirred at rt for 3 h. Mixture was concentrated to dryness. Dichloroethane (ca. 10 mL) was added, and the mixture was back concentrated to dryness to obtain crude (2-bromo-5-methoxy-4-methyl-phenyl)-acetic acid chloride (151 mg).

후처리

  1. concentrationMixture was concentrated to dryness
  2. additionDichloroethane (ca. 10 mL) was added
  3. concentrationthe mixture was back concentrated to dryness

출처 및 근거

ORD 기록
ord-ac473a77240f48d9a5d40899e3546efe
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153808B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트