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Water → Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate

HRID 704701
ノート
印刷プレビュー

反応式

HRID 704701 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 14575268Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate収率 69.3%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

(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).

後処理

  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

出典と根拠

ORDレコード
ord-2c4b2377b9434d5dbf427fc64674738e
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04988689

反応ノート

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