HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365782Generated: October 30, 2026
Triethyl phosphite → (+/-)-2-Diethoxyphosphinoyl-5-(p-Toluenesulfonyloxymethyl)-Tetrahydrofuran
https://huagongshe.com/reaction/365782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (+/-)-2-Acetoxy-5-(p-Toluenesulfonyloxymethyl)-Tetrahydrofuran | HCID 21255879 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+/-)-2-Diethoxyphosphinoyl-5-(p-Toluenesulfonyloxymethyl)-Tetrahydrofuran | HCID 21255867 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127540 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-b0bbcd7f2f0448e883415f917715ab11 |
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| Source note | uspto-grants-2000_10 |
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