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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365770Generated: October 31, 2026

Triphenylphosphine → HCID 131720782, compound

https://huagongshe.com/reaction/365770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 21255857HCID 21255857—
ReactantHCID 178418634HCID 178418634—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131720782HCID 13172078262%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of triphenylphosphine (101 g, 385 mmol, 2 eq) in THF (1.5 L) was added diisopropylazodicarboxylate (76 mL, 386 mmol, 2 eq) at 0° C. The mixture was stirred at 0° C. for 1 hr and was followed by the addition of a solution of methyl 3-t-butyldiphenylsilyloxy-2-hydroxypropionate (example 39) (68.89 g, 192 mmol) and thioacetic acid (27.6 mL, 386 mmol, 2 eq.) in THF, to the same temperature. The mixture was stirred at 0° C. for 1 hr and at room temperature for 18 hr. The solution was concentrated to dryness and the solid was washed with hexane (5×300 mL). The organic solution was filtered and evaporated under reduced pressure. The crude material was purified by flash chromatography with a mixture of hexane and ethyl acetate (95:5) to give the pure compound (49.3 g) in 62% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127540
Source datasetuspto-grants-2000_10
ORD IDord-b486b383c21d4aaf8cdda66ab74b59ef
Source noteuspto-grants-2000_10