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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571063Generated: October 30, 2026

Thionyl Chloride → 5-(benzyloxy)-2-(chloromethyl)-4H-pyran-4-one

https://huagongshe.com/reaction/571063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-(benzyloxy)-2-(hydroxymethyl)-4H-pyran-4-oneHCID 901598—
SolventDiethyl EtherHCID 3283—
Product5-(benzyloxy)-2-(chloromethyl)-4H-pyran-4-oneHCID 3703321—

Reaction Steps

To a suspension of 5-(benzyloxy)-2-(hydroxymethyl)-4H-pyran-4-one (18.5 g, 80 mmol) in Et2O (130 mL) was added SOCl2 (18 mL, 110 mmol) at r.t. and the mixture was stirred for 1 h. The reaction mixture was poured onto ice-water and more Et2O was added. Then the Et2O phase was collected and water phase was extracted by Et2O twice, the combined Et2O layer was washed with brine, dried over Na2SO4, and concentrated. The residue was purified by silica gel chromatography to give 5-(benzyloxy)-2-(chloromethyl)-4H-pyran-4-one 1HNMR (DMSO, 400 MHZ) δ 8.27 (s, 1H), 7.32-7.41 (m, 5H), 6.55 (s, 1H), 4.92 (s, 2H), 4.65 (s, 2H). MS (M+H)+ 250.1/252.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024032B2
Source datasetuspto-grants-2015_05
ORD IDord-7615938a76884ad1b976d4abd7a643f5
Source noteuspto-grants-2015_05