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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500594Generated: November 1, 2026

Phenol → (S)-Tert-Butyl 3-phenoxypyrrolidine-1-carboxylate

https://huagongshe.com/reaction/500594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylateHCID 6544479—
SolventTetrahydrofuranHCID 8028—
Product(S)-Tert-Butyl 3-phenoxypyrrolidine-1-carboxylateHCID 6933348575%

Reaction Steps

Di-isopropylazodicarboxylate (5.7 mL, 29.38 mmol) was added to an ice-cooled solution of (R)-(−)-N-boc-3-pyrrolidinol (5 g, 26.71 mmol), phenol (2.51 g, 26.71 mmol) and triphenyl phosphine (7.71 g, 29.38 mmol) in tetrahydrofuran (70 mL) and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated in vacuo and the residue was twice triturated with diethyl ether and filtered. The filtrate was washed with 1N sodium hydroxide solution (20 mL), dried over sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane:ethyl acetate, 90:10 to 83:17, afforded the title compound as a colourless oil in 75% yield, 5.27 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772223B2
Source datasetuspto-grants-2010_08
ORD IDord-fb9c7ec8d5464c28ac4b2c694139b232
Source noteuspto-grants-2010_08