Tetrahydrofuran → trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol
反応式
[O:1]1[CH:11]2[CH:2]1[CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([OH:12])[C:9]=1[CH2:10]2.[O:13]1CCCC1.Cl(O)(=O)(=O)=O.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl.CCOCC.O>[C:8]1([OH:12])[C:9]2[CH2:10][C@@H:11]([OH:1])[C@H:2]([OH:13])[CH2:3][C:4]=2[CH:5]=[CH:6][CH:7]=1参加物
実験手順
A solution of 8.0 g. (0.048 mole) of 5,6,7,8-tetrahydro-6,7-epoxy-1-naphthol in 100 ml. of tetrahydrofuran is cooled to 0° and 20 ml. of water and 0.5 ml. of 70% perchloric acid are added. After 4 hr., a further 1.5 ml. of acid is added and the solution stirred for 16 hr. at ambient temperature and diluted with 100 ml. each of ether, 10% sodium bicarbonate and saturated salt solution. The aqueous layer is separated and washed with 150 ml. of 1:1 ether-tetrahydrofuran. The organic phase is washed with saturated salt solution, dried and evaporated to give an oil which solidifies on trituration with chloroform. Recrystallization gives in two crops, 4.85 g. of solid which is recrystallized from ethyl acetate to give 3.84 g. m.p. 179.5°-181.5°. Two further recrystallizations of a small sample give the analytical specimen, m.p. 183°-184°.
後処理
- additionof acid is added
- additionat ambient temperature and diluted with 100 ml
- customThe aqueous layer is separated
- washwashed with 150 ml
- washThe organic phase is washed with saturated salt solution
- customdried
- customevaporated
- customto give an oil which
- customRecrystallization
- customgives in two crops, 4.85 g
- customof solid which is recrystallized from ethyl acetate
- customto give 3.84 g
- customTwo further recrystallizations of a small sample
- customgive the analytical specimen, m.p. 183°-184°
出典と根拠
- ORDレコード
- ord-f0496fda9bca4f0ea323f0a730f12c94
- 出典データセット
- uspto-grants-1976_09
- 特許番号
- US03982021
反応ノート
読み込み中…