Water → Ethyl morpholinoethyl 3-trifluoromethylbenzylphosphonate

HRID 1733822ノート

反応式

HRID 1733822 の反応式
[CH2:1]([O:3][P:4]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=1)(Cl)=[O:5])[CH3:2].[OH:18][CH2:19][CH2:20][N:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1.C(N(CC)CC)C.O>C(Cl)Cl>[F:17][C:14]([F:15])([F:16])[C:10]1[CH:9]=[C:8]([CH:13]=[CH:12][CH:11]=1)[CH2:7][P:4](=[O:5])([O:18][CH2:19][CH2:20][N:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1)[O:3][CH2:1][CH3:2]

参加物

6

反応物 4

HCID 962WaterHCID 8471TriethylamineHCID 611632-MorpholinoethanolHCID 158191953-Trifluoromethylbenzylphosphonochloridic acid ethyl ester

生成物 1

HCID 15818099Ethyl morpholinoethyl 3-trifluoromethylbenzylphosphonate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

3-Trifluoromethylbenzylphosphonochloridic acid ethyl ester (7.0 mmol)in 20 mL of CH2Cl2 is added slowly to a mixture of N-(2-hydroxyethyl)morpholine and triethylamine (7 mmol) in 20 mL of CH2Cl2 cooled in an ice bath. The resultant mixture is allowed to reach room temperature and is stirred for 5 hours. Water is added (100 mL) and the aqueous phase is extracted 3 times with CH2Cl2 (3×100 mL). The combined organic extracts are dried with anhydrous MgSO4, and evaporated to give the desired product.

後処理

  1. temperaturecooled in an ice bath
  2. customto reach room temperature
  3. extractionthe aqueous phase is extracted 3 times with CH2Cl2 (3×100 mL)
  4. dry with materialThe combined organic extracts are dried with anhydrous MgSO4
  5. customevaporated

出典と根拠

ORDレコード
ord-b9a01b15cf394c678d84216bc5754ffa
出典データセット
uspto-grants-1996_07
特許番号
US05532226

反応ノート

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