Sodium Iodide → 3-(2-Naphthalenylmethoxy)-α-pentylbenzenemethanol
反応式
Br[CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1.[OH:13][CH:14]([C:20]1[CH:21]=[C:22]([OH:26])[CH:23]=[CH:24][CH:25]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].C(=O)([O-])[O-].[Cs+].[Cs+]>CC(C)=O>[OH:13][CH:14]([C:20]1[CH:21]=[C:22]([CH:23]=[CH:24][CH:25]=1)[O:26][CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]参加物
7
実験手順
A suspension of 2-bromomethyl naphthalene (5 g, 0.023 mol), 3-(1-hydroxyhexyl)phenol (5 g, 0.026 mol), powdered potassium carbonate (4.5 g, 0.033 mol), sodium iodide (0.4 g, 0.0023 mol) and cesium carbonate (0.7 g, 0.0021 mol) in dry acetone (75 ml) was refluxed overnight (14 hours). The reaction mixture was filtered, the filtrate was concentrated, dissolved in ether, and then washed successively with 1N NaOH solution 6N HCl solution, water and brine. After drying the organics over anhydrous MgSO4, all volatiles were removed. The crude product (5 g) was further purified by chromatography, using 8% ethylacetate in hexanes on silica gel, to yield 3.5 g of the pure desined compound as a colorless liquid.
後処理
- temperaturewas refluxed overnight (14 hours)
- filtrationThe reaction mixture was filtered
- concentrationthe filtrate was concentrated
- dissolutiondissolved in ether
- washwashed successively with 1N NaOH solution 6N HCl solution, water and brine
- dry with materialAfter drying the organics over anhydrous MgSO4
- customall volatiles were removed
- customThe crude product (5 g) was further purified by chromatography
- customto yield 3.5 g of the
出典と根拠
- ORDレコード
- ord-940045f476264268b22b274eab05092b
- 出典データセット
- uspto-grants-1988_10
- 特許番号
- US04778931
反応ノート
読み込み中…