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

S-(o-Nitrophenyl)-N-acetyl-D-cysteine → S-(o-Nitrophenyl)-D-cysteine

HRID 53119
노트
인쇄 미리보기

반응식

HRID 53119 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][CH2:11][C@H:12]([C:17]([OH:19])=[O:18])[NH:13]C(=O)C)([O-:3])=[O:2]>S(=O)(=O)(O)O>[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][CH2:11][C@H:12]([C:17]([OH:19])=[O:18])[NH2:13])([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 13375098S-(o-Nitrophenyl)-N-acetyl-D-cysteine

생성물 1

HCID 13375100S-(o-Nitrophenyl)-D-cysteine수율 100%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

반응 조건

온도
0 °C

실험 절차

A solution of 13.6 g (47.9 mmol) of S-(o-nitrophenyl)-N-acetyl-D-cysteine was refluxed in 57 mL of 18M sulfuric acid (H2SO4) for 1 hour. The bright yellow solution was cooled to 0° C. and concentrated. Ammonium hydroxide (NH4OH) was added to adjust the pH=5.4. The resulting precipitate was filtered and dried to yield 11.6 g (100% ) of product.

후처리

  1. concentrationconcentrated
  2. additionAmmonium hydroxide (NH4OH) was added
  3. filtrationThe resulting precipitate was filtered
  4. customdried

출처 및 근거

ORD 기록
ord-b7167f9134904423ae762dc2aecb6d72
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05618808

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트