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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methanol → Methyl 2-amino-3-(thiophen-2-yl)propanoate hydrochloride

HRID 255622
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반응식

HRID 255622 반응식
S(Cl)([Cl:3])=O.[CH3:5]O.Cl.[S:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[CH2:13][CH:14]([C:16]([OH:18])=[O:17])[NH2:15]>>[ClH:3].[CH3:5][O:17][C:16](=[O:18])[CH:14]([CH2:13][C:9]1[S:8][CH:12]=[CH:11][CH:10]=1)[NH2:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 201658013-(2-thienyl)-DL-alanine hydrochloride

생성물 1

HCID 67438693Methyl 2-amino-3-(thiophen-2-yl)propanoate hydrochloride수율 100.1%

실험 절차

3.78 g (0.0318 mole) of thionyl chloride were added dropwise at -5° C. to 10.2 g (0.318 mole) of methanol. After 5 minutes, 3.3 g (0.0159 mole) of 3-(2-thienyl)-DL-alanine hydrochloride were added gradually to this solution, whilst keeping the temperature at -5° C. The mixture was then stirred for 3 hours at this temperature, and then left standing for 24 hours at room temperature. The reaction product was then condensed by evaporation under reduced pressure, and ethanol was added to the residue. The mixture was then condensed by evaporation under reduced pressure and 3.53 g (yield 100%) of 3-(2-thienyl)-DL-alanine methyl ester hydrochloride melting at 110°-112° C. were obtained as the residue.

후처리

  1. customat -5° C
  2. waitleft
  3. waitstanding for 24 hours at room temperature
  4. customcondensed
  5. customby evaporation under reduced pressure, and ethanol
  6. additionwas added to the residue
  7. customcondensed
  8. customby evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-b1f06b06f8e6482da9b20ed123e3053b
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04698329

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