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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481346Generated: October 30, 2026

Benzyl Alcohol → Benzyl oxolan-3-ylcarbamate

https://huagongshe.com/reaction/481346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant(R)-Tetrahydro-3-furoic acidHCID 4661317—
Solvent1,4-DioxaneHCID 31275—
ProductBenzyl oxolan-3-ylcarbamateHCID 2186452551.2%

Reaction Steps

A mixture of 3-tetrahydrofuroic acid (3.5 gm, 30 mmol), diphenylphosphorylazide (6.82 ml, 32 mmol), triethylamine (5 ml, 36 mmol) in dioxane (35 ml) was stirred at RT for 20 min then heated in a 100° C. oil bath under dry nitrogen for 2 hours. Benzyl alcohol (4.7 ml, 45 mmol) was added, and continued heating at 100° C. for 22 hours. The mixture was cooled, filtered from a white precipitate and concentrated. The residue was dissolved in 2N HCI and extracted twice using EtOAc. The extracts were washed with water, sodium bicarbonate, brine dried over MgSO4, and then concentrated to an oil which solidifies upon standing. The oil was chromatographed (30% to 60% EtOAc/Hex) to give 3.4 g of an oil (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789416
Source datasetuspto-grants-1998_08
ORD IDord-c15d9c2a8d7d4793951ee2e3b6757706
Source noteuspto-grants-1998_08