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2-Amino-1-[3-(trifluoromethyl)phenyl]ethan-1-ol → N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine

HRID 851499
ノート
印刷プレビュー

反応式

HRID 851499 の反応式
[OH:1][CH:2]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1)[CH2:3][NH2:4].[C:15]([C:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][C:27](=O)[CH3:28])=[CH:21][CH:20]=1)([O:17][CH3:18])=[O:16].[BH4-].[Na+]>C1C=CC=CC=1.CO>[C:15]([C:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][CH:27]([NH:4][CH2:3][CH:2]([OH:1])[C:5]2[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:12])([F:13])[F:14])[CH:6]=2)[CH3:28])=[CH:21][CH:20]=1)([O:17][CH3:18])=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 305142-Amino-1-[3-(trifluoromethyl)phenyl]ethan-1-olHCID 4311764Sodium borohydrideHCID 109326404-(3-Oxobutyl)benzoic acid methyl ester

生成物 1

HCID 20493837N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine

試薬・触媒・溶媒 2

HCID 241Benzene溶媒
HCID 887
Methanol
溶媒

実験手順

A solution of 2-hydroxy-2-(3-trifluoromethylphenyl) ethanamine (3 g) and 4-(4-carbomethoxyphenyl)butan-2-one (3 g) in benzene was boiled for 21/2 hours with azeotropic removal of water and then evaporated to give an oil which was dissolved in methanol and this solution was treated with sodium borohydride (2 g) at 0° C. After 2 hours the solution was evaporated, diluted with water and extracted with dichloromethane and the product from the dried (MgSO4) organic extracts was chromatographed on silica gel eluting with 5% methanol in chloroform to yield the title compound as an oil; 1H n.m.r. τ(CDCl3) 2.00-2.90 (m, 8H); 5.33 (m,1H); 6.12 (s,3H); 6.92-7.57 (m,7H; 2H exchangeable on D2O wash); 8.16-8.50 (m,2H); 8.91 (d,3H). The product was isolated as the hydrochloride salt m.p. 147.5°-150.5° C., as a 55:45 mixture of diastereoisomers.

後処理

  1. custom2 hours
  2. customwith azeotropic removal of water
  3. customevaporated
  4. customto give an oil which
  5. customAfter 2 hours the solution was evaporated
  6. additiondiluted with water
  7. extractionextracted with dichloromethane
  8. dry with materialthe product from the dried (MgSO4) organic extracts
  9. customwas chromatographed on silica gel eluting with 5% methanol in chloroform

出典と根拠

ORDレコード
ord-3edfbf36c7674220bbf33ce99710dacb
出典データセット
uspto-grants-1983_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04385066

反応ノート

読み込み中…

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