tert-Butanol → tert-Butyl 3-(3-(1-allyl-1H-1,2,3-triazol-4-yl)phenethoxy)propanoate

HRID 909920ノート

反応式

HRID 909920 の反応式
[CH:1]1(Br)[CH2:3][CH2:2]1.[C:5]([C:7]1[CH:8]=[C:9]([CH:22]=[CH:23][CH:24]=1)[CH2:10][CH2:11][O:12][CH2:13][CH2:14][C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])#[CH:6].[N-:25]=[N+:26]=[N-:27].[Na+].C(O)(C)(C)C>C(OCC)(=O)C.N.[Cu]I.O>[CH2:2]([N:25]1[CH:6]=[C:5]([C:7]2[CH:8]=[C:9]([CH:22]=[CH:23][CH:24]=2)[CH2:10][CH2:11][O:12][CH2:13][CH2:14][C:15]([O:17][C:18]([CH3:20])([CH3:21])[CH3:19])=[O:16])[N:27]=[N:26]1)[CH:1]=[CH2:3]

参加物

9

反応条件

温度
70 °C

実験手順

Cyclopropyl bromide (0.177 mL) was added in one portion to a mixture tert-butyl 3-(3-ethynylphenethoxy)propanoate [Example 4, Step ii)] (506 mg), sodium azid e (144 mg), tert-butanol (0.5 mL), water (2 mL) and copper(I) iodide (35.1 mg) and sealed into a microwave tube. The reaction was heated to 70° C., over a period of 3 h in the microwave reactor. The reaction mixture was diluted with ethyl acetate and 35% ammonia (1 mL) and ethyl acetate (2 mL) were added. The mixture was stirred for 30 min. and extracted into ethyl acetate. The organic was evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 20 to 100% ethyl acetate in isohexane to afford the titled compound (470 mg) as an oil. 1H NMR (400 MHz, CDCl3) δ 7.78 (s, 1H), 7.70 (s, 1H), 7.66 (d, J=7.9 Hz, 1H), 7.33 (t, J=7.7 Hz, 1H), 7.19 (d, J=7.7 Hz, 1H), 6.08 (ddt, J=5.9, 10.3 and 16.9 Hz, 1H), 5.41-5.32 (m, 2H), 5.03 (dt, J=6.2, 1.3 Hz, 2H), 3.70 (t, J=6.3 Hz, 2H), 3.69 (t, J=7.1 Hz, 2H), 2.92 (t, J=7.0 Hz, 2H), 2.48 (t, J=6.5 Hz, 2H), 1.43 (s, 9H)

後処理

  1. customsealed into a microwave tube
  2. additionwere added
  3. extractionextracted into ethyl acetate
  4. customThe organic was evaporated
  5. customto afford crude product
  6. customThe crude product was purified by flash silica chromatography, elution gradient 20 to 100% ethyl acetate in isohexane

出典と根拠

ORDレコード
ord-3a602e44beb343259188e2d1cc6828b5
出典データセット
uspto-grants-2011_09
特許番号
US08017602B2

反応ノート

読み込み中…