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Carbon Disulfide → Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate

HRID 704703
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HRID 704703 반응식
O1CCCC1.[NH2:6][CH:7]1[CH2:11][CH2:10][N:9]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:8]1.[C:17](=S)=[S:18]>>[N:6]([CH:7]1[CH2:11][CH2:10][N:9]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:8]1)=[C:17]=[S:18]
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참가 물질

4

반응물 3

HCID 6348Carbon DisulfideHCID 8028TetrahydrofuranHCID 13656208Ethyl 3-aminopyrrolidine-1-carboxylate

생성물 1

HCID 14575268Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate수율 99.8%

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온도
-10 °C

실험 절차

(a-3) To a stirred and cooled (10° C.) mixture of 37 parts of N,N-methane-tetraylbis[cyclohexanamine] and 594 parts of tetrahydrofuran were added 91.2 parts of carbon disulfide. After cooling to -10° C., 27.5 parts of ethyl 3-aminopyrrolidinecarboxylate were added during a period of 5 minutes (exothermic reaction). The reaction mixture was allowed to reach room temperature and evaporated. The residue was purified by column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated, yielding 32 parts (99.8%) of ethyl 3-isothiocyanato-1-pyrrolidinecarboxylate as a residue (interm. 6).

후처리

  1. temperaturecooled
  2. custom(exothermic reaction)
  3. customto reach room temperature
  4. customevaporated
  5. customThe residue was purified by column chromatography over silica gel
  6. customThe pure fractions were collected
  7. customthe eluent was evaporated

출처 및 근거

ORD 기록
ord-c0d29c014c734bbe88dd0d58c3be6463
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04988689

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