N-Benzylformamide → Ethyl N-Benzylformimidate

HRID 224415

反応式

HRID 224415 の反応式
[CH2:1]([NH:8][CH:9]=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.F[B-](F)(F)F.[CH2:16]([O+](CC)CC)[CH3:17]>C(Cl)Cl>[CH2:1]([N:8]=[CH:9][O:10][CH2:16][CH3:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

4

実験手順

A solution of 690 mg (5.1 mmoles) of N-benzylformamide in 5 ml of methylene chloride is cooled in an ice-water bath and put under an argon blanket. The solution is stirred while 4.9 ml (4.9 mmoles) of 1 M triethyloxonium fluoroborate in methylene chloride is added dropwise. After a 45 minute reaction time, the mixture is concentrated to dryness under reduced pressure at room temperature, and the residue is dried under reduced pressure over P2O5. The nuclear magnetic resonance spectrum of the product in deuterochloroform is fully in accord with the product being a fluoroborate etherate complex of ethyl N-benzylformimidate.

後処理

  1. additionis added dropwise
  2. customAfter a 45 minute reaction time
  3. concentrationthe mixture is concentrated to dryness under reduced pressure at room temperature
  4. dry with materialthe residue is dried under reduced pressure over P2O5

出典と根拠

ORDレコード
ord-a595cc6d8e3144d39967fc2d45eb7a60
出典データセット
uspto-grants-1980_11
特許番号
US04232030

関連ノート

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