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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763054Generated: November 3, 2026

Dichloromethane → HCID 14280461, compound

https://huagongshe.com/reaction/1763054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantHCID 14280459HCID 14280459—
CatalystBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14280461HCID 14280461121.2%

Reaction Steps

200 mg (1.06 mmol) of methyl (+)-3-hydroxy-2,4-dimethylheptanoate (+)-(4) was dissolved in 4 ml of tetrahydrofuran, and 134 mg (1.59 mmol) of dihydropyran and 1 mg of pyridinium p-toluenesulfonate were added, and the mixture was reacted overnight at room temperature. Since TLC (Thin Layer Chromatography) showed that the starting materials still remained, 5 mg of pyridinium p-toluenesulfonate and 3 ml of methylene chloride were added, and the reaction was further carried out overnight at room temperature. The reaction mixture was extracted with ether. The ethereal layer was washed with a saturated aqueous solution of sodium hydrogencarbonate and then with an aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate, filtered, and concentrated to give 350 mg of crude methyl (+)-2,4-dimethyl-3-tetrahydropyranyloxy-1-heptanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835292
Source datasetuspto-grants-1989_05
ORD IDord-2c77f05425714e6eba63d689e7136ab7
Source noteuspto-grants-1989_05