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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712507Generated: November 3, 2026

3,4-dihydro-2H-pyran → 6-(Tetrahydropyran-2-yloxymethyl)-4H-benzo[1,4]oxazin-3-one

https://huagongshe.com/reaction/1712507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant6-(Hydroxymethyl)-2H-1,4-benzoxazin-3(4H)-oneHCID 18452443—
SolventDichloromethaneHCID 6344—
Product6-(Tetrahydropyran-2-yloxymethyl)-4H-benzo[1,4]oxazin-3-oneHCID 68503993—

Reaction Steps

The solution of 5.0 g of 6-hydroxymethyl-4H-benzo[1,4]oxazin-3-one in 60 ml of dichloromethane is admixed successively with 5.20 ml of 3,4-dihydro-2H-pyran and 0.236 g of p-toluenesulphonic acid monohydrate. The reaction mixture is stirred at room temperature over 14 hours. The solution is poured onto 1M sodium hydrogencarbonate solution (300 ml) and extracted with tert-butyl methyl ether (2×400 ml). The organic phase is washed with brine (300 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a beige solid from the residue by means of crystallization (EtOAc/heptane). Rf=025 (1:1 EtOAc-heptane); Rt=3.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-fa690dcb2a6940ef8ae9143ea7ff01b5
Source noteuspto-grants-2010_09