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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481722Generated: October 30, 2026

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

https://huagongshe.com/reaction/481722

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 Celite. 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 750 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 numberUS05789394
Source datasetuspto-grants-1998_08
ORD IDord-f8360605921e40fa941a3b16b5ee61d7
Source noteuspto-grants-1998_08