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Hydrochloric Acid → N-{3-[(1-Chloro-2-nitroethenyl)sulfanyl]propyl}acetamide

HRID 371344
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인쇄 미리보기

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HRID 371344 반응식
[OH-].[Na+].[SH:3][CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:10])[CH3:9].[Cl:11][C:12](Cl)=[CH:13][N+:14]([O-:16])=[O:15].Cl.[Cl-].[Na+]>CO>[Cl:11][C:12]([S:3][CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:10])[CH3:9])=[CH:13][N+:14]([O-:16])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 14798Sodium HydroxideHCID 122195711,1-Dichloro-2-nitroetheneHCID 20238484N-(3-Mercaptopropyl)acetamide

생성물 1

HCID 53674132N-{3-[(1-Chloro-2-nitroethenyl)sulfanyl]propyl}acetamide

시약·촉매·용매 1

실험 절차

A solution of 0.12 g of sodium hydroxide in 5 ml of methanol was added over 10 minutes to a solution of 0.40 g of 1 in 5 ml of methanol. Then a solution of 0.95 g of 1,1-dichloro-2-nitroethene (13A) in 5 ml of methanol was added over 20 minutes, at 0° C. The mixture then was stirred for 20 minutes and poured into 2% hydrochloric acid saturated with sodium chloride. The resulting mixture was extracted with methylene chloride, the solvent was evaporated and the residue was purified over silica gel to give 13, as an oil.

후처리

  1. extractionThe resulting mixture was extracted with methylene chloride
  2. customthe solvent was evaporated
  3. customthe residue was purified over silica gel

출처 및 근거

ORD 기록
ord-1bcf7bbb274a4fd9b42c1a7daa22b0fd
출처 데이터셋
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04531002

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 887
Methanol
용매
3회