関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2-[2-(Hydroxymethyl)phenyl]ethanol | HCID 239024 | — |
| 反応物 | Lithium Chloride | HCID 433294 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl ester | HCID 54328826 | 45% |
反応手順
Mix 2-(2-hydroxymethyl-phenyl)-ethanol (12.0 g, 78.8 mmol) and collidine (23 mL, 0.17 mol) and treat with lithium chloride (7.35 g, 0.173 mmol) in dimethylformamide (125 mL). Cool in an ice bath and treat, by dropwise addition, with mesyl chloride (13.4 mL). Stir at 0° C. for 4 hours, partition between ice water (300 mL) and a 1:1 mixture of ether:pentane (2×400 mL). Wash the organic layer with a saturated solution of CuSO4 (2×200 mL), dry (MgSO4) and purify by silica gel chromatography (2.5:1 hexane/ethyl acetate followed by 2:1 hexane/ethyl acetate followed by 3:2 hexane/ethyl acetate) to give the title compound as a pale yellow oil (8.8 g, 45%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05731306 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-d530a516b02640fda96b3ced16ffaeab |
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| 出典メモ | uspto-grants-1998_03 |
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