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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270911Generated: October 30, 2026

Water → 2-(3-Butynyloxy)tetrahydro-2H-pyran

https://huagongshe.com/reaction/1270911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant3-Butyn-1-OLHCID 13566—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventDichloromethaneHCID 6344—
Product2-(3-Butynyloxy)tetrahydro-2H-pyranHCID 14244098%

Reaction Steps

A solution of but-3-yn-1-ol (10.00 g, 143 mmol) in dichloromethane (310 mL) was treated with dihyropyran (18.10 g, 215 mmol) and pyridinium p-toluene sulfonate (3.60 g, 14.30 mmol). The reaction mixture was stirred at room temperature for 4 days. Water was added and the layers were partitioned. The organic layer was washed with brine, dried over magnesium sulfate, filtered and evaporated under reduced pressure. The crude material was purified by flash chromatography on silica gel using 1:1 ethyl acetate:heptane to give 21.57 g (98%) of the title compound. 1H NMR (CDCl3, 400 MHz) δ 4.65 (m, 1H), 3.90–3.80 (m, 2H), 3.60–3.50 (m, 2H), 2.50–2.45 (m, 2H), 1.95 (m, 1H), 1.90–1.80 (m, 1H), 1.79–1.10 (m, 1H), 1.65–1.50 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202363B2
Source datasetuspto-grants-2007_04
ORD IDord-91310ceffa164648ba11e7466d5bcf4d
Source noteuspto-grants-2007_04