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Tert-Butylamine → Carbamate

HRID 1992335
ノート
印刷プレビュー

反応式

HRID 1992335 の反応式
Cl[C:2](Cl)([O:4][C:5](=[O:11])OC(Cl)(Cl)Cl)Cl.[C:13]([NH2:17])([CH3:16])([CH3:15])[CH3:14].C(N(CC)CC)C.[Br:25][CH2:26][CH2:27][OH:28]>C(Cl)Cl.CN(C1C=CN=CC=1)C.O>[C:5](=[O:11])([O-:4])[NH2:17].[C:13]([NH:17][C:2](=[O:4])[O:28][CH2:27][CH2:26][Br:25])([CH3:16])([CH3:15])[CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 6385Tert-ButylamineHCID 8471TriethylamineHCID 108982-BromoethanolHCID 94429Triphosgene

生成物 2

HCID 276CarbamateHCID 179479972-Bromoethyl tert-butylcarbamate

試薬・触媒・溶媒 3

HCID 14284
4-(Dimethylamino)pyridine
触媒
HCID 962Water溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

To a cooled solution of triphosgene (76 g, 0.256 mol, 0.75 eq.) in dry DCM (150 mL) was added, dropwise at 0° C. over a period of 3 hrs under a N2 atmosphere, a mixture of tert-butylamine (25 g, 0.3418 mol, 1.0 eq.), DMAP (2.08 g, 0.017 mol, 0.05 eq.) and triethylamine (67.1 g, 0.6836 mol, 2.0 eq.) in dry DCM (100 mL). After addition of the mixture was complete, the reaction mixture was stirred at RT for 12 hrs. The reaction mixture was cooled to 0° C. and 2-bromoethanol (106.8 g, 0.854 mol, 2.5 eq.) was added. The reaction mixture was then stirred at RT for 6 hrs, before being diluted with water and extracted with DCM. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and then concentrated under reduced pressure. The resulting residue was distilled under reduced pressure to yield carbamate the sub-title compound as a colourless liquid. Yield: 28 g.

後処理

  1. additionAfter addition of the mixture
  2. temperatureThe reaction mixture was cooled to 0° C.
  3. stirringThe reaction mixture was then stirred at RT for 6 hrs
  4. extractionextracted with DCM
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. distillationThe resulting residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-2d81cabefa5d445ea9318b972dfb4ec8
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07648985B2

反応ノート

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