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Water → Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate

HRID 704701
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HRID 704701 반응식
[C:1](Cl)(Cl)=[S:2].O.[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(=O)([O-])[O-].[Ca+2]>ClC(Cl)Cl>[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:1]=[S:2]
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참가 물질

6

반응물 4

HCID 962WaterHCID 10040ThiophosgeneHCID 10112Calcium CarbonateHCID 13656208Ethyl 3-aminopyrrolidine-1-carboxylate

생성물 1

HCID 14575268Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate수율 69.3%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

(a-1) To a stirred mixture of 25 parts of carbonothioic dichloride, 65 parts of water and 210 parts of trichloromethane were added dropwise 9.3 parts of ethyl 3-aminopyrrolidinecarboxylate. Upon completion, the reaction mixture was stirred for 15 minutes at room temperature. 10.7 Parts of calcium carbonate were added portionwise during a period of 10 minutes and stirring was continued overnight at room temperature. The reaction mixture was filtered and the separated organic layer was dried, filtered 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. The residue was distilled at 6.65 Pa, yielding 7.5 parts (69.3%) of ethyl 3-isothiocyanato-1-pyrrolidinecarboxylate; bp. 101° C. (interm 6).

후처리

  1. stirringstirring
  2. waitwas continued overnight at room temperature
  3. filtrationThe reaction mixture was filtered
  4. customthe separated organic layer was dried
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was purified by column chromatography over silica gel
  8. customThe pure fractions were collected
  9. customthe eluent was evaporated
  10. distillationThe residue was distilled at 6.65 Pa

출처 및 근거

ORD 기록
ord-2c4b2377b9434d5dbf427fc64674738e
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04988689

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