Water → 3-Methylindene
反応式
O[C:2]1([CH3:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3]1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1.O>C1(C)C=CC=CC=1>[CH3:11][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]=1参加物
5
実験手順
A solution of 24.64 (0.166 mol) of 1-hydroxy-1-methyl-2,3-dihydro-1H-indene and 0.30 g of p-toluenesulphonic acid monohydrate in 300 ml of toluene was heated to reflux for 3 h with water being collected by means of a Dean Stark trap. The reaction mixture was cooled, washed with water (3×100 ml), then with saturated sodium chloride solution (100 ml), dried (K2CO3) and evaporated in vacuo to leave an orange oil. This was vacuum distilled to yield 14.57 g (67%) of the title product as a colourless oil, b.p. 32°-35° C./0.3 mm of Hg. NMR δ(CDCl3) 2.17 (3H, m), 3.31 (2H, m), 6.20 (1H, m), 7.16-7.35 (3H, m), 7.45 (1H, m).
後処理
- customcollected by means of a Dean Stark trap
- temperatureThe reaction mixture was cooled
- washwashed with water (3×100 ml)
- dry with materialwith saturated sodium chloride solution (100 ml), dried (K2CO3)
- customevaporated in vacuo
- customto leave an orange oil
- distillationThis was vacuum distilled
出典と根拠
- ORDレコード
- ord-22a755d67a1a4dba8491066187c2026a
- 出典データセット
- uspto-grants-1993_10
- 特許番号
- US05254561
反応ノート
読み込み中…