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Potassium Carbonate → tert-butyl[(2S,3E)-1-{[tert-butyl(diphenyl)silyl]oxy}-4-(2-nitrophenyl)but-3-en-2-yl]carbamate

HRID 714127
ノート
印刷プレビュー

反応式

HRID 714127 の反応式
[C:1]([O:5][C:6](=[O:30])[NH:7][C@@H:8]([CH:28]=O)[CH2:9][O:10][Si:11]([C:24]([CH3:27])([CH3:26])[CH3:25])([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([CH3:4])([CH3:3])[CH3:2].[Br-].[N+:32]([C:35]1[CH:60]=[CH:59][CH:58]=[CH:57][C:36]=1[CH2:37][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O-:34])=[O:33].[PH4+].C(=O)([O-])[O-].[K+].[K+].C1OCCOCCOCCOCCOCCOC1>COCCOC.C(Cl)Cl>[C:1]([O:5][C:6](=[O:30])[NH:7][C@@H:8](/[CH:28]=[CH:37]/[C:36]1[CH:57]=[CH:58][CH:59]=[CH:60][C:35]=1[N+:32]([O-:34])=[O:33])[CH2:9][O:10][Si:11]([C:24]([CH3:25])([CH3:26])[CH3:27])([C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([CH3:3])([CH3:4])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 11430Potassium CarbonateHCID 2855718-Crown-6HCID 5460504PhosphoniumHCID 10885283(2-Nitrobenzyl)triphenylphosphonium bromideHCID 89929680tert-butyl[(2R)-1-{[tert-butyl(diphenyl)silyl]oxy}-3-oxopropan-2-yl]carbamate

生成物 1

HCID 131734057
tert-butyl[(2S,3E)-1-{[tert-butyl(diphenyl)silyl]oxy}-4-(2-nitrophenyl)but-3-en-2-yl]carbamate
収率 38.1%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 80711,2-Dimethoxyethane溶媒

実験手順

A solution of tert-butyl[(2R)-1-{[tert-butyl(diphenyl)silyl]oxy}-3-oxopropan-2-yl]carbamate (3, 3.12 g, 7.3 mmol) in DME (30 ml) was treated with solid (2-nitrobenzyl)(triphenyl)phosphonium bromide(3.76 g, 7.86 mmol) (or any other suitable phosphonium salt), the mixture stirred at room temperature under N2 atmosphere for 30 min and then the reaction flask was charged with a solid mixture of potassium carbonate (1.78 g, 12.86 mmol) and 18-crown-6 (219 mg, 0.83 mmol). The purple mixture was further stirred at the same temperature for 14 h; diluted with DCM, washed with saturated NaHCO3, dried over MgSO4, filtered and concentrated Purified through a chromatographic cartridge of silicagel (50 g) eluted with 10% to 35% EtOAc in hexane to get 1.52 g (38% yield) of title compound as light yellow oil. MS: m/z=569.2 (MNa+).

後処理

  1. stirringThe purple mixture was further stirred at the same temperature for 14 h
  2. washwashed with saturated NaHCO3
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customPurified through a chromatographic cartridge of silicagel (50 g)
  7. washeluted with 10% to 35% EtOAc in hexane

出典と根拠

ORDレコード
ord-13cfa7bc3a9f4e0a87920188b63cd6d6
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187415B2

反応ノート

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