Water → 1-(4-Propoxyphenyl)-2-propanone
反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9](=[O:11])[CH3:10])=[CH:4][CH:3]=1.Br[CH2:13][CH2:14][CH3:15].C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O>[CH2:13]([O:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9](=[O:11])[CH3:10])=[CH:6][CH:7]=1)[CH2:14][CH3:15]参加物
6
実験手順
A suspension of 15.0 g of 1-(4-hydroxyphenyl)-2-propanone, 24.6 g of 1-bromopropane and 13.8 g of potassium carbonate in 100 ml of N,N-dimethylformamide was heated for 4 hours at 65°-70° C. After cooling, the reaction mixture was poured into water and extracted with ether. The extract was washed with water, dried and evaporated. The residue was distilled to give 15.2 g of the desired compound as a pale yellow oil, b.p.136°-138° C. (7 mmHg).
後処理
- temperaturewas heated for 4 hours at 65°-70° C
- temperatureAfter cooling
- extractionextracted with ether
- washThe extract was washed with water
- customdried
- customevaporated
- distillationThe residue was distilled
出典と根拠
- ORDレコード
- ord-d76effe29391474dad3987c18fdedf54
- 出典データセット
- uspto-grants-1990_11
- 特許番号
- US04971990
反応ノート
読み込み中…