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

Dimethyl Sulfate → Methyl 2,4-dichloro-3-(1'-methoxyimino-1-(methoxy)methyl)benzoate

HRID 377547
노트
인쇄 미리보기

반응식

HRID 377547 반응식
[Cl:1][C:2]1[C:11]([C:12]([NH:14][O:15][CH3:16])=[O:13])=[C:10]([Cl:17])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:18](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CN(C)C=O>[Cl:1][C:2]1[C:11]([C:12](=[N:14][O:15][CH3:16])[O:13][CH3:18])=[C:10]([Cl:17])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl Sulfate2회HCID 11430Potassium CarbonateHCID 18517407Methyl 2,4-dichloro-3-methoxyaminocarbonylbenzoate

생성물 1

HCID 53659114Methyl 2,4-dichloro-3-(1'-methoxyimino-1-(methoxy)methyl)benzoate수율 11.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 16.0 g (0.058 mol) of methyl 2,4-dichloro-3-methoxyaminocarbonylbenzoate and 10.1 g (0.073 mol) of potassium carbonate in 300 ml of dimethylformamide was stirred for 30 minutes at room temperature. 11.0 g (0.087 mol) of dimethyl sulfate were subsequently added dropwise, the mixture was stirred for 12 hours at room temperature, and another 11.0 g of dimethyl sulfate were added. After the mixture had been heated for 6 hours at 60° C., it was cooled and stirred into 2 l of ice-water. Then, the aqueous phase was extracted with ethyl acetate, the combined organic phases were dried and the solvent was distilled off in vacuo. After chromatography of the residue on silica gel (eluant:toluene/ethyl acetate=9/1), 2.0 g of methyl 2,4-dichloro-3-(1'-methoxyimino-1'-(methoxy)methyl)benzoate were obtained.

후처리

  1. stirringthe mixture was stirred for 12 hours at room temperature
  2. temperatureAfter the mixture had been heated for 6 hours at 60° C.
  3. temperatureit was cooled
  4. extractionThen, the aqueous phase was extracted with ethyl acetate
  5. customthe combined organic phases were dried
  6. distillationthe solvent was distilled off in vacuo

출처 및 근거

ORD 기록
ord-66b20f9e23c14cd8844274d71612d04f
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06028035

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트