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Methanol → Carbamic acid, N-(4-amino-1-methylcyclohexyl)-, 1,1-dimethylethyl ester

HRID 869243
ノート
印刷プレビュー

反応式

HRID 869243 の反応式
[CH3:1][C:2]1([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.CO.C([O-])=O.[NH4+:22]>[Pd].O>[NH2:22][CH:5]1[CH2:6][CH2:7][C:2]([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:1])[CH2:3][CH2:4]1
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 887MethanolHCID 2723923Ammonium formateHCID 21882608tert-butyl N-(1-methyl-4-oxocyclohexyl)carbamate

生成物 1

HCID 20754832Carbamic acid, N-(4-amino-1-methylcyclohexyl)-, 1,1-dimethylethyl ester収率 92.8%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 962
Water
溶媒

実験手順

To a mixture of tert-butyl (1-methyl-4-oxocyclohexyl)carbamate (4.00 g) and methanol (50 mL), ammonium formate (10.2 g) and water (5 mL) were added and stirred for 1 hour until they were completely dissolved. Then, 10% palladium on carbon (2.0 g) was added and stirred at room temperature for 65 hours. After insoluble materials were separated by filtration through celite, the solvent was distilled off, and chloroform was added to the resulting residue, followed by drying over anhydrous magnesium sulfate. The solvent was distilled off to give tert-butyl (4-amino-1-methylcyclohexyl)carbamate (3.73 g) as a colorless syrup.

後処理

  1. additionwere added
  2. dissolutionwere completely dissolved
  3. stirringstirred at room temperature for 65 hours
  4. customAfter insoluble materials were separated by filtration through celite
  5. distillationthe solvent was distilled off
  6. additionchloroform was added to the resulting residue
  7. dry with materialby drying over anhydrous magnesium sulfate
  8. distillationThe solvent was distilled off

出典と根拠

ORDレコード
ord-2cbd4b36e7ae45179ab9477a99b5524e
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969336B2

反応ノート

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