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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908960Generated: October 28, 2026

Triphenylphosphine → HCID 86661405, compound

https://huagongshe.com/reaction/1908960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactanttert-Butyl (3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoateHCID 11616071—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86661405HCID 8666140573.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.90 g of triphenylphosphine and 15 mL of tetrahydrofuran were added to 100 mL flask and the resulting reaction solution was cooled to 0° C. 2.17 mL of diisopropylazodicarboxylate was dropped while the reaction solution was stirred. After 30 minutes, 10 mL of tetrahydrofuran solution with 1.52 g of (S)-t-butyl 3-(t-butoxycarbonylamino)-4-hydroxybutanoate was dropped and stirred for 16 hours while the reaction temperature was naturally increased to room temperature. After completing the reaction, 40 mL of ethyl acetate and 40 mL of water were added to the reaction solution and then stirred for 10 minutes. An organic layer was isolated, dehydrated with magnesium sulfate, and then concentrated under reduced pressure. A concentrated residue was isolated with column chromatography (n-hexane:ethyl acetate=15:1) and then concentrated under reduced pressure to obtain 1.04 g of a title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598347B2
Source datasetuspto-grants-2013_12
ORD IDord-c67559a558e540b7b72ed3374ccc11f6
Source noteuspto-grants-2013_12