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Carbon Disulfide → Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate

HRID 704703
ノート
印刷プレビュー

反応式

HRID 704703 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

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

生成物 1

HCID 14575268Ethyl 3-isothiocyanatopyrrolidine-1-carboxylate収率 99.8%

反応条件

温度
-10 °C

実験手順

(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).

後処理

  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

出典と根拠

ORDレコード
ord-c0d29c014c734bbe88dd0d58c3be6463
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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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート