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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284317Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 357800, compound

https://huagongshe.com/reaction/1284317

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantEthyl 6-hydroxyhexanoateHCID 357781—
SolventDichloromethaneHCID 6344—
ProductHCID 357800HCID 357800—

Reaction Steps

66 g. (0.412 mol) of ethyl 6-hydroxyhexanoate [prepared as described by S. R. Sandler and W. Karo, in `Organic Functional Group Preparation` , Academic Press, New York, and London, vol. 1, page 262. (cf. G. B. Hatch and H. Adkins, J. Am. Chem. Soc., 59 1694 (1937))] were dissolved in 400 ml. of methylene chloride, and the mixture was reacted with 45 g. of dihydropyran and 1 g. of p-toluenesulphonic acid at 25°C. for 20 minutes. The reaction mixture was washed with an aqueous sodium bicarbonate solution, dried and concentrated. The residue was distilled in vacuo to obtain 77 g. of the title compound having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978229
Source datasetuspto-grants-1976_08
ORD IDord-0f7632a4a0e54e04b08429a5f769b3db
Source noteuspto-grants-1976_08