Triethylamine → HCID 44544858、化合物

HRID 391254ノート

反応式

HRID 391254 の反応式
P(Br)(Br)Br.[Cl:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12][C:13]([OH:15])=[O:14].[Br:16]Br.[O:18]=[C:19]([N:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1)[C@H:20](O)[CH3:21].C(N(CC)CC)C.[OH-].[Na+]>O.C1(C)C=CC=CC=1>[Br:16][CH:12]([C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=1[Cl:5])[C:13]([O:15][C@H:20]([CH3:21])[C:19](=[O:18])[N:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1)=[O:14]

参加物

9

反応条件

温度
50 °C

実験手順

To phosphorus tribromide (28 g, 103.4 mmol), 2-chlorophenylacetic acid (44 g, 257.9 mmol) was added. The mixture was stirred at 50° C. for 1 hour. After stirring, bromine (66 g, 413.0 mmol) was added thereto at the same temperature for reaction overnight. After the reaction, toluene (200 mL) and (2R)-1-oxo-1-pyrrolidinylpropane-2-ol (40.6 g, 283.6 mmol) were added thereto at the same temperature. Subsequently, triethylamine (34 g, 336.0 mmol) was added thereto to carry out reaction for 2 hours. After the reaction, water was added thereto. After the mixture was neutralized with a 30% sodium hydroxide aqueous solution, the organic layer was separated from the water layer and the water layer was disposed of. The obtained organic layer was washed with water, and the water layer was separated and disposed of. The organic layer was concentrated under reduced pressure to obtain 83.1 g of the target compound (221.8 mmol, 86%).

後処理

  1. stirringAfter stirring
  2. customat the same temperature for reaction overnight
  3. additionwere added
  4. customreaction for 2 hours
  5. additionwas added
  6. customthe organic layer was separated from the water layer
  7. washThe obtained organic layer was washed with water
  8. customthe water layer was separated
  9. concentrationThe organic layer was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-bb3f5046be184fe1897458afbad647d5
出典データセット
uspto-grants-2013_02
特許番号
US08383833B2

反応ノート

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