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HRID 1075309作成日:2026年10月25日

3,4-dihydro-2H-pyran → 3-Chloro-2-tetrahydropyranyloxy-1-propyl acetate

https://huagongshe.com/reaction/1075309

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物3-Chloro-2-hydroxypropyl acetateHCID 98069—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
溶媒DichloromethaneHCID 6344—
生成物3-Chloro-2-tetrahydropyranyloxy-1-propyl acetateHCID 19048416—

反応手順

A solution of 271.9 g (1.78 moles) of 3-chloro-2-hydroxy-1-propyl acetate, 244 ml (2.67 moles) of freshly distilled dihydropyran, and 44.7 g (0.178 moles) of pyridinium p-toluenesulfonate in 1800 mL of methylene chloride was stirred at room temperature with cooling to control the reaction exotherm. After 22 hours the reaction mixture was washed with 500 mL of water and 250 mL of sodium chloride solution, and was dried over sodium sulfate. Solvent was removed and the residue was dried at 0.03 mm for 1.5 hours to give 473.3 g of crude 3-chloro-2-tetrahydropyranyloxy-1-propyl acetate: 1H NMR (CDCl3) δ1.63 (br. s, 6 H, (CH2)3); 2.08 (s, 3H, CH3CO); 3.5-4.3 (7H, CH2CHCH2); 4.73 (br. s, 1H, --O--CH); IR (neat, NaCl) 3000, 2910 (C--H); 1740 cm- 1 (--O--CO--CH3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04395561
出典データセットuspto-grants-1983_07
ORD IDord-6da761fed5ce46139d12240f4f8561a4
出典メモuspto-grants-1983_07