化工社化工社 化学情報印刷レポート · 研究参考用
Thionyl Chloride → 5-(Chloromethyl)-2,3-dihydro-1h-indene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | (2,3-dihydro-1H-inden-5-yl)methanol | HCID 330183 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 5-(Chloromethyl)-2,3-dihydro-1h-indene | HCID 233149 | 99% |
反応手順
Thionyl chloride (120 ml, 1.65 mol) was added drop-wise to a rapidly stirred mixture of (2,3-dihydro-1H-inden-5-yl)methanol (81.4 g, 0.55 mol) in chloroform (500 ml) at 0° C. After the addition was complete, the resulting mixture was allowed to warm to room temperature and the stirring was continued for an additional 12 h. The chloroform was evaporated under reduced pressure to give a residue, that was purified by column chromatography (petroleum ether:ethyl acetate=15:1) to afford 5-(chloromethyl)-2,3-dihydro-1H-indene (90.5 g, 99%). 1H NMR (300 MHz, CDCl3) δ 2.06-2.19 (m, 4H), 2.93 (t, J=7.5, 4H), 4.54 (s, 2H), 7.15-7.31 (m, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08969386B2 |
| 出典データセット | uspto-grants-2015_03 |
| ORD ID | ord-4a3756c987734f16ae59478bb5fb46b7 |
| 出典メモ | uspto-grants-2015_03 |