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HRID 2707作成日:2026年10月24日

2,4,6-Trimethylpyridine → Methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl ester

https://huagongshe.com/ja/reaction/2707

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2-[2-(Hydroxymethyl)phenyl]ethanolHCID 239024—
反応物Lithium ChlorideHCID 433294—
溶媒DimethylformamideHCID 6228—
生成物Methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl esterHCID 5432882645%

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731306
出典データセットuspto-grants-1998_03
ORD IDord-d530a516b02640fda96b3ced16ffaeab
出典メモuspto-grants-1998_03