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Hydrochloric Acid → 1-Cyano-1-(2-methoxy-3,5-dibromophenyl)cyclohexane

HRID 444102
ノート
印刷プレビュー

反応式

HRID 444102 の反応式
[H-].[Na+].Br[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]Br.[Br:10][C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[C:13]([CH2:18][C:19]#[N:20])[C:12]=1[O:21][CH3:22].Cl>CN(C)C=O.O>[C:19]([C:18]1([C:13]2[CH:14]=[C:15]([Br:17])[CH:16]=[C:11]([Br:10])[C:12]=2[O:21][CH3:22])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)#[N:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 81001,5-DibromopentaneHCID 24758Sodium hydrideHCID 205361852,4-Dibromo-6-cyanomethylanisole

生成物 1

HCID 205362401-Cyano-1-(2-methoxy-3,5-dibromophenyl)cyclohexane

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒
2 回

実験手順

To a stirred suspension of sodium hydride (7 g) in dry dimethylformamide (200 ml) was added a solution of 1,5-dibromopentane (20 ml) and the product of stage (d) in dimethylformamide (40 ml), keeping the temperature at 20°-30° C. The mixture was stirred for 30 minutes, water was added cautiously, and was then poured into ice water. Hydrochloric acid was added and the mixture was extracted with dichloromethane, washed with water and brine, dried over magnesium sulphate and filtered, and the solvent was removed to give a pale brown oil which slowly crystallised. Recrystallisation from ethanol gave the title product as yellow crystalls, mp 100°-102° C.

後処理

  1. customat 20°-30° C
  2. extractionthe mixture was extracted with dichloromethane
  3. washwashed with water and brine
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customthe solvent was removed
  7. customto give a pale brown oil which
  8. customslowly crystallised
  9. customRecrystallisation from ethanol

出典と根拠

ORDレコード
ord-85f5274eb87044a296136b774044700d
出典データセット
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04263037

反応ノート

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