Potassium Carbonate → tert-butyl N-[1-(N'-hydroxycarbamimidoyl)-1-methylethyl]carbamate

HRID 632013ノート

反応式

HRID 632013 の反応式
C(=O)([O-])[O-].[K+].[K+].[Cl-].[OH:8][NH3+:9].[C:10]([C:12]([NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:14])[CH3:13])#[N:11]>O.C(O)C>[NH2:11]/[C:10](=[N:9]\[OH:8])/[C:12]([NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:14])[CH3:13]

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 21645Hydroxylamine HClHCID 18316698tert-butyl N-(1-cyano-1-methylethyl)carbamate

生成物 1

HCID 61324195tert-butyl N-[1-(N'-hydroxycarbamimidoyl)-1-methylethyl]carbamate収率 94.1%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

Potassium carbonate (3.64 g) was dissolved in water (12 mL) and hydroxylammonium chloride (CAN: 5470-11-1, 1.7 g, mmol) was added. A solution of tert-butyl 2-cyanopropan-2-ylcarbamate (4.84 g, 26 mmol) in ethanol (42 mL) was added and the resulting reaction mixture was stirred for 18 h at ambient temperature. The solvent was removed under reduced pressure and the residue was diluted with ethyl acetate (20 mL). The mixture was filtered and the filtrate was concentrated to yield the crude product (5 g, 87.6%) as yellow solid. MS: m/e=218.2 [M+H]+.

後処理

  1. customthe resulting reaction mixture
  2. customThe solvent was removed under reduced pressure
  3. additionthe residue was diluted with ethyl acetate (20 mL)
  4. filtrationThe mixture was filtered
  5. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-cb74553367e540f789dbb65aec0200e3
出典データセット
uspto-grants-2016_04
特許番号
US09321727B2

反応ノート

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