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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636878Generated: October 31, 2026

Triethyl phosphite → (+/-)-2-Diethoxyphosphinoyl-5-(p-Toluenesulfonyloxymethyl)-Tetrahydrofuran

https://huagongshe.com/reaction/636878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphiteHCID 31215—
ReactantSodium BicarbonateHCID 516892—
Reactant(+/-)-2-Acetoxy-5-(p-Toluenesulfonyloxymethyl)-TetrahydrofuranHCID 21255879—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product(+/-)-2-Diethoxyphosphinoyl-5-(p-Toluenesulfonyloxymethyl)-TetrahydrofuranHCID 21255867—

Reaction Conditions

Temperature-35 °C

Reaction Steps

To a stirring solution of (±)-2-acetoxy-5-(p-toluenesulfonoxymethyl)-tetrahydrofuran (example 59) (1.63 g, 5.19 mmol) and triethyl phosphite (1.16 mL, 6.75 mmol) in methylene chloride (75 mL) at −35° C. was added titanium (IV) chloride (0.57 mL, 5.19 mmol) dropwise. The yellow solution was then stirred at −35° C. for 30 min and then at 0° C. for 30 min. Saturated NaHCO3 (75 mL) was then added to the reaction mixture and the suspension was then filtered through a CELITE diatomaceous earth. The mixture was then partitioned followed by extraction of the aqueous phase with methylene chloride (2×50 mL). The combined extracts were then washed with brine (100 mL), dried (MgSO4) and concentrated. The residue was then purified by chromatography eluting with 75% EtAc/hexanes-EtAc giving the title compound as 1:1 mixture of cis and trans isomers (1.42 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194576B1
Source datasetuspto-grants-2001_02
ORD IDord-b567e5779ee14541ba82ae1ca3fb6450
Source noteuspto-grants-2001_02