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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010475Generated: October 31, 2026

Ammonium Chloride → Tert-butyl 3-hydroxy-3-phenylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1010475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
ProductTert-butyl 3-hydroxy-3-phenylpyrrolidine-1-carboxylateHCID 6666256949.24%

Reaction Steps

To a solution of tert-butyl 3-oxopyrrolidine-1-carboxylate (1 g, 5.40 mmol) in ether (20 ml) was added dropwise phenylmagnesium bromide (10.3 mL, 3.0 M in ether, 6.21 mmol) at rt under nitrogen. The reaction was heated to reflux for 15 min, then cooled to rt, poured into sat. NH4Cl, extracted with ether (3×). The combined organic layers were dried over Na2SO4, concentrated in vacuo. The crude residue was purified by flash column chromatography to yield the desired product (700 mg, 49.24%). LCMS (M+H) 264.160.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973041B2
Source datasetuspto-grants-2011_07
ORD IDord-3b09a0a16d2944d3b009ff424730467d
Source noteuspto-grants-2011_07