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

Oxalyl chloride → 3,4,5-Trimethoxyphenyl-2-oxoacetyl chloride

HRID 2415045
노트
인쇄 미리보기

반응식

HRID 2415045 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13](=[O:17])[C:14](O)=[O:15])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].C(Cl)(=O)C([Cl:21])=O>C(Cl)Cl.CN(C)C=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13](=[O:17])[C:14]([Cl:21])=[O:15])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 111283972-oxo-2-(3,4,5-trimethoxyphenyl)acetic Acid

생성물 1

HCID 226400793,4,5-Trimethoxyphenyl-2-oxoacetyl chloride

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매2회

실험 절차

A stirred suspension of 3,4,5-trimethoxyphenyl-2-oxoacetic acid (1.60 g, 6.66 mmoles) in dry methylene chloride (26 mL) at room temperature was treated with 2M oxalyl chloride in methylene chloride (14 mL, 4 equiv.) and dry dimethylformamide (1 drop). After 3 h the solvents were evaporated. The residue was flushed with dry methylene chloride (3×50 mL) and dried in vacuo for 2 h during which time a solid formed. The crude acid chloride was carried on without further purification.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customAfter 3 h the solvents were evaporated
  2. customThe residue was flushed with dry methylene chloride (3×50 mL)
  3. customdried in vacuo for 2 h during which time a solid
  4. customformed
  5. customThe crude acid chloride was carried on without further purification

출처 및 근거

ORD 기록
ord-30d3d369eb614c6bb7827fe36fdc3b8d
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06818643B1

반응 노트

불러오는 중…