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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695322Generated: October 31, 2026

Triphenylphosphine → HCID 57570897, compound

https://huagongshe.com/reaction/1695322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanttris(2hydroxyethyl)methaneHCID 12053840—
ReactantHCID 178418634HCID 178418634—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57570897HCID 5757089737.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of triphenylphosphine (1.77 g, 6.8 mmol) in anhydrous THF (15 mL) was added diethyl azodicarboxylate (2.2 M in toluene, 2.4 mL, 5.4 mmol) dropwise at 0° C. After stirred at 0° C. for 55 minutes, a solution of 3-(2-hydroxyethyl)pentane-1,5-diol (740 mg, 5 mmol) and thioacetic acid (335 μL, 4.5 mmol) in dry THF (7 mL) was added dropwise. After 1 hour the ice/water bath was removed and the reaction was stirred at room temperature for 16 hours. The solvents were removed by rotary evaporation in vacuo. The residue was purified by flash chromatography (CHCl3/MeOH, 20:1, 15:1, 10:1, 4:1) to give 3-(2-acetylthioethyl)pentane-1,5-diol as white solid (350 mg) and recovered starting material triol (406 mg). 1H NMR (400 Hz, CDCl3): δ 3.65-3.63 (m, 4H), 3.45 (bs, 2H), 2.84-2.80 (m, 2H), 2.28 (s, 3H), 1.73-1.67 (m, 1H), 1.55-1.49 (m, 6H). MS (ESI): m/z 229.0 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163736B2
Source datasetuspto-grants-2012_04
ORD IDord-44f1b7c4eaf04bc19a73864ba7009ec9
Source noteuspto-grants-2012_04