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

Methanol → HCID 69331780, 화합물

HRID 1374983
노트
인쇄 미리보기

반응식

HRID 1374983 반응식
S(Cl)([Cl:3])=O.Cl.[CH3:6][O:7][C:8]1[CH:9]=[C:10]([CH:17]=[CH:18][C:19]=1[CH3:20])[CH2:11][C@H:12]([C:14]([OH:16])=[O:15])[NH2:13].[CH3:21]O>>[ClH:3].[CH3:21][O:15][C:14](=[O:16])[C@@H:12]([CH2:11][C:10]1[CH:17]=[CH:18][C:19]([CH3:20])=[C:8]([O:7][CH3:6])[CH:9]=1)[NH2:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl Chloride2회HCID 69331765HCID 69331765, 화합물

생성물 1

HCID 69331780HCID 69331780, 화합물

실험 절차

Thionyl chloride (0.7 ml) was added dropwise to a solution of 3-methoxy-4-methyl-D-phenylalanine hydrochloride (1.75 g) in methanol (8 ml) over 10 minutes at room temperature. The whole was stirred at 40–50° C. for 2 hours and then an additional thionyl chloride (0.7 ml) was added to the mixture. The whole mixture was stirred for further 1 hour and evaporated under reduced pressure. The resulting solid was triturated with diisopropyl ether and collected by filtration to give colorless crystals of 3-methoxy-4-methyl-D-phenylalanine methyl ester hydrochloride (1.70 g).

후처리

  1. stirringThe whole mixture was stirred for further 1 hour
  • customevaporated under reduced pressure
  • customThe resulting solid was triturated with diisopropyl ether
  • filtrationcollected by filtration
  • 출처 및 근거

    ORD 기록
    ord-a6a37df20b3b4a339af7001d15b6716d
    출처 데이터셋
    uspto-grants-2007_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07166598B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트