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

(Chlorothio)formyl chloride → 5-Methoxymethyl-1,3,4-oxathiazol-2-one

HRID 618197
노트
인쇄 미리보기

반응식

HRID 618197 반응식
Cl[C:2]([S:4]Cl)=[O:3].[CH3:6][O:7][CH2:8][C:9]([NH2:11])=[O:10]>C1(C)C=CC=CC=1>[CH3:6][O:7][CH2:8][C:9]1[O:10][C:2](=[O:3])[S:4][N:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 75990(Chlorothio)formyl chlorideHCID 1400602-Methoxyacetamide

생성물 1

HCID 218503335-Methoxymethyl-1,3,4-oxathiazol-2-one수율 79.9%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
95 °C

실험 절차

Chlorocarbonylsulfenyl chloride (7.35 g) was added to a suspension of methoxyacetamide (5 g) in toluene (30 cm3). The reaction mixture was stirred and heated at 90-100° C. for 5 hours, then cooled. The solvent was removed by evaporation under reduced pressure to give a brown gum (6.6 g). M+ =147; 1H NMR (DMSO-d6): δ3.30(3H,s); 4.30(2H,s) which was used in the next step without further purification.

후처리

  1. temperaturecooled
  2. customThe solvent was removed by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-117b7970d9404edba40b1dbf73a5d195
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05952359

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트