Water → 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride

HRID 974545

反応式

HRID 974545 の反応式
[C:1]([Cl:4])(Cl)=[O:2].C(=O)([O-])[O-].[K+].[K+].C1(C(C2C=CC=CC=2)[N:18]2[CH2:21][CH:20]([O:22][C:23]3[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=3)[CH2:19]2)C=CC=CC=1.O>C(Cl)Cl>[F:29][C:26]1[CH:27]=[CH:28][C:23]([O:22][CH:20]2[CH2:19][N:18]([C:1]([Cl:4])=[O:2])[CH2:21]2)=[CH:24][CH:25]=1

参加物

6

実験手順

A solution of 52.09 g (0.527 mole) of phosgene in 500 ml of methylene chloride was stirred with 73 g (0.53 mole) of potassium carbonate under nitrogen atmosphere for 30 min, then treated with 146.3 g (0.439 mole) of 1-diphenylmethyl-3-(4-fluorophenoxy)azetidine in 300 ml of methylene chloride added dropwise. After stirring for 18 hr, the reaction mixture was treated with 200 ml of water added slowly. The aqueous phase was separated and the organic solution dried by filtration through Whatman phase separating filter paper then concentrated in vacuo to a pale amber oil. Trituration of the oil with 30/60 petroleum ether yielded a crude tacky solid, 89.3 g (88.6%). A portion of this solid was recrystallized from 30/60 petroleum ether yielding a fine white crystalline product, m.p. 44°-52° C. A second recrystallization from isopropyl ether yielded fine white crystals, m.p. 57°-58.5° C.

後処理

  1. additionadded dropwise
  2. additionadded slowly
  3. customThe aqueous phase was separated
  4. customthe organic solution dried by filtration through Whatman phase
  5. customseparating
  6. filtrationfilter paper
  7. concentrationthen concentrated in vacuo to a pale amber oil
  8. customTrituration of the oil with 30/60 petroleum ether yielded a crude tacky solid, 89.3 g (88.6%)
  9. customA portion of this solid was recrystallized from 30/60 petroleum ether yielding a fine white crystalline product, m.p. 44°-52° C
  10. customA second recrystallization from isopropyl ether yielded fine white crystals, m.p. 57°-58.5° C.

出典と根拠

ORDレコード
ord-c79644b79d5a48aea1c5f779fe3709ef
出典データセット
uspto-grants-1991_11
特許番号
US05068231

関連ノート

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