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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1075309Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1075309

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-dihydro-2H-pyranHCID 8080—
Edukt3-Chloro-2-hydroxypropyl acetateHCID 98069—
EduktBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Chloro-2-tetrahydropyranyloxy-1-propyl acetateHCID 19048416—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04395561
Quelldatensatzuspto-grants-1983_07
ORD IDord-6da761fed5ce46139d12240f4f8561a4
Quellennotizuspto-grants-1983_07