Triethylamine → HCID 25179430, 화합물

HRID 2101262노트

반응식

HRID 2101262 반응식
[CH3:1][Si:2]([CH3:12])([CH3:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.Cl.[F:14][C:15]([F:27])([F:26])[O:16][C:17]1[CH:18]=[C:19]([CH2:23][CH2:24][NH2:25])[CH:20]=[CH:21][CH:22]=1.C(N(CC)CC)C.[BH4-].[Na+]>CO.O>[F:14][C:15]([F:26])([F:27])[O:16][C:17]1[CH:18]=[C:19]([CH2:23][CH2:24][NH:25][CH2:7][C:6]2[CH:9]=[CH:10][C:3]([Si:2]([CH3:12])([CH3:11])[CH3:1])=[CH:4][CH:5]=2)[CH:20]=[CH:21][CH:22]=1

참가 물질

7

반응물 4

HCID 8471TriethylamineHCID 6375734-(Trimethylsilyl)benzaldehydeHCID 4311764Sodium borohydrideHCID 574385032-[3-(Trifluoromethoxy)phenyl]ethan-1-amine hydrochloride

생성물 1

HCID 25179430HCID 25179430, 화합물수율 100.7%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

4-Trimethylsilanyl-benzaldehyde (178 mg, 1 mmol), 2-(3-trifluoromethoxy-phenyl)-ethyl-amine hydrochloride (241 mg, 1.1 mmol) and triethyl amine (151 mg, 1.5 mmol) were dissolved in methanol (5 ml) and the solution was stirred at rt for 5 min. Sodium borohydride (37 mg, 1 mmol) was added under nitrogen and the reaction mixture was stirred at rt for 1 h. Water was added and methanol was evaporated in vacuo. The reaction was extracted twice with diethyl ether and the combined organic layers were washed once with water and once with sat. aq. NaCl solution, dried with sodium sulfate, filtered off and concentrated in vacuo to yield [2-(3-trifluoromethoxy-phenyl)-ethyl]-(4-trimethylsilanyl-benzyl)-amine (370 mg, 100%) as a colorless oil. MS (ISP) 368.2 (100) (M+H)+.

후처리

  1. stirringthe reaction mixture was stirred at rt for 1 h
  2. custommethanol was evaporated in vacuo
  3. extractionThe reaction was extracted twice with diethyl ether
  4. washthe combined organic layers were washed once with water and once with sat. aq. NaCl solution
  5. dry with materialdried with sodium sulfate
  6. filtrationfiltered off
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9fce47b64154467ebe06bb2fd9e7f25d
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07572823B2

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