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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595329Generated: October 30, 2026

Iodine → 4-[(Benzyloxy)methyl]-5-(iodomethyl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/595329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBenzyl [1-(benzyloxy)but-3-en-2-yl]carbamateHCID 12180511—
SolventDichloromethaneHCID 6344—
SolventSodium ThiosulfateHCID 24477—
Product4-[(Benzyloxy)methyl]-5-(iodomethyl)-1,3-oxazolidin-2-oneHCID 13567472—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of benzyl [1-(benzyloxy)but-3-en-2-yl]carbamate (3.0 g, 9.6 mmol) and iodine (4.9 g, 19 mmol) in dichloromethane (200 mL) was stirred at 20° C. for 16 hours. The reaction mixture was diluted with aqueous sodium thiosulfate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the crude product residue. The crude product residue was purified by silica gel chromatography (ethyl acetate/petroleum ether) to give 4-[(benzyloxy)methyl]-5-(iodomethyl)-1,3-oxazolidin-2-one. MS ESI calc'd. for C12H15INO3 [M+H]+ 348. found 348. 1H NMR (300 MHz, CDCl3) δ 7.40-7.27 (m, 5H), 5.53 (s, 1H), 4.57 (s, 2H), 4.37-4.34 (m, 1H), 3.82-3.80 (m, 1H), 3.67-3.51 (m, 2H), 3.38-3.32 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-3570c4be1b924f539521e5d284cfe153
Source noteuspto-grants-2016_01