Ammonium Chloride → HCID 69134565、化合物

HRID 917684ノート

反応式

HRID 917684 の反応式
[Mg].Br[C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([O:13][CH3:14])[CH:9]=2)[CH:4]=1.[CH2:15]([O:22][CH:23]1[CH2:28][CH2:27][C:26](=[O:29])[CH:25]([CH2:30][N:31]([CH3:33])[CH3:32])[CH2:24]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[Cl-].[NH4+]>C1COCC1>[CH2:15]([O:22][CH:23]1[CH2:28][CH2:27][C:26]([C:3]2[CH:12]=[CH:11][C:10]3[C:5](=[CH:6][CH:7]=[C:8]([O:13][CH3:14])[CH:9]=3)[CH:4]=2)([OH:29])[CH:25]([CH2:30][N:31]([CH3:33])[CH3:32])[CH2:24]1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

参加物

6

実験手順

The corresponding Grignard reagent was produced in 11 ml THF p.a. from 0.28 g magnesium and 2.72 g 2-bromo-6-methoxynaphthalene, a solution of 2.00 g 4-benzyloxy-2-dimethylaminomethylcyclohexanone in 8 ml THF p.a. added dropwise with ice cooling, and the mixture stirred for 1 hour. For working up, 4 ml 4 M ammonium chloride solution were added to the ice bath, the organic phase separated off, the aqueous phase extracted twice with diethyl ether, the combined organic phases dried by sodium sulphate, filtered and concentrated. The crude product obtained (3.20 g) was chromatographed with ethyl acetate/methanol/hexane (V/V/V=1:1:1) on silica gel. 1.52 g 4-benzyloxy-2-dimethylaminomethyl-1-(6-methoxynaphthalen-2-yl)cyclohexanol were obtained and converted into the corresponding hydrochloride (1.32 g) in the same way as in AAV 1.

後処理

  1. additionadded dropwise with ice cooling
  2. customthe organic phase separated off
  3. extractionthe aqueous phase extracted twice with diethyl ether
  4. dry with materialthe combined organic phases dried by sodium sulphate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product obtained (3.20 g)
  8. customwas chromatographed with ethyl acetate/methanol/hexane (V/V/V=1:1:1) on silica gel

出典と根拠

ORDレコード
ord-55ba57b8eb7c4ae49047ea4d02fd3f6f
出典データセット
uspto-grants-2007_09
特許番号
US07273952B2

反応ノート

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