ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Triphenylphosphine → Tert-butyl (1s,2r)-1-benzyl-2-hydroxyhexylcarbamate

HRID 1987149
ノート
印刷プレビュー

反応式

HRID 1987149 の反応式
[CH2:1]([C@H:8]([NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19])[C@H:9]([OH:14])[CH2:10][CH2:11][CH2:12][CH3:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[NH:42]=[N+:43]=[N-:44].CCOC(/N=N/C(OCC)=O)=O>C1COCC1>[CH2:1]([C@H:8]([NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19])[C@H:9]([OH:14])[CH2:10][CH2:11][CH2:12][CH3:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N:42]([C@@H:9]([CH2:10][CH2:11][CH2:12][CH3:13])[C@@H:8]([NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19])[CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[N+:43]=[N-:44]
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 11776TriphenylphosphineHCID 24530Hydrazoic acidHCID 5462977Diethyl azodicarboxylateHCID 90726167Tert-butyl (1s,2r)-1-benzyl-2-hydroxyhexylcarbamate2 回

生成物 2

HCID 90726167Tert-butyl (1s,2r)-1-benzyl-2-hydroxyhexylcarbamateHCID 90893745HCID 90893745、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of tert-butyl (1S,2R)-1-benzyl-2-hydroxyhexylcarbamate (1.24 g, 4.03 mmol), triphenylphosphine (1.06 g, 4.03 mmol) in 40 mL THF was added hydrozoic acid HN3 (4 mL, 8.07 mmol, 2M in benzene) followed by dropwise addition of diethylazodicarboxylate (0.7 mL, 4.44 mmol) in 10 mL THF. The reaction mixture was stirred at room temperature for 8 h, combined with a previous 250 mg tert-butyl (1S,2R)-1-benzyl-2-hydroxyhexylcarbamate probe reaction, concentrated in vacuo, and purified by flash chromatography (120 g silica, 0−>50% EtOAc/hexanes) to afford tert-butyl (1S,2R)-1-benzyl-2-hydroxyhexylcarbamate and tert-butyl (1S,2S)-2-azido-1-benzylhexylcarbamate as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.36-7.16 (m, 5H), 4.63 (d, J=10.1 Hz, 1H), 4.00-3.88 (m, 1H), 3.40-3.28 (m, 1H), 2.91 (A of ABX, dd, J=13.6, 6.8 Hz, 1H), 2.76 (B of ABX, dd, J=13.6, 9.1 Hz, 1H), 1.70-1.48 (m, 2H), 1.42-1.20 (m, 4H), 1.39 (s, 9H), 0.52 (t, J=7.1 Hz, 3H).

後処理

  1. concentrationconcentrated in vacuo
  2. custompurified by flash chromatography (120 g silica, 0−>50% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-0e10ce1cc14448a78eb05a602bc161b8
出典データセット
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07550481B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート