化工社化工社 化学情報印刷レポート · 研究参考用
Isobutylene oxide → 1-(4-Bromo-2-methoxyphenoxy)-2-methylpropan-2-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isobutylene oxide | HCID 11208 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Trisodium Phosphate | HCID 24243 | — |
| 反応物 | 4-Bromo-2-methoxyphenol | HCID 262234 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 1-(4-Bromo-2-methoxyphenoxy)-2-methylpropan-2-ol | HCID 59595049 | 92.1% |
反応手順
A mixture of 4-bromo-2-methoxyphenol (8 g, 39.4 mmol), 2,2-dimethyloxirane (14 mL, 158 mmol), potassium carbonate (4.3 g, 35.5 mmol), and sodium phosphate, monobasic (4.25 g, 35.5 mmol) in acetonitrile and water (85:15, 100 mL) was stirred in a steel bomb at 150-165° C. for 8 h. The reaction was cooled to RT, diluted with ether and EtOAc (1:1), washed with 1N NaOH, dried (Na2SO4), and concentrated. The crude was passed through a pad of silica gel using EtOAc for elution to afford the desired product 1-(4-bromo-2-methoxyphenoxy)-2-methylpropan-2-ol 9A (10 g, 36.3 mmol, 92% yield) as a brown oil. 1H NMR (400 MHz, Chloroform-d) δ6.95-7.08 (2H, m), 6.77 (1H, d, J=8.28 Hz), 3.85 (3H, s), 3.79 (2H, s), 1.34 (6H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08563583B2 |
| 出典データセット | uspto-grants-2013_10 |
| ORD ID | ord-9121703c7ed543eab7622c8c1dfd3050 |
| 出典メモ | uspto-grants-2013_10 |