Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535031Generated: October 30, 2026

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

https://huagongshe.com/reaction/535031

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 (3x). 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 numberUS08853243B2
Source datasetuspto-grants-2014_10
ORD IDord-aa1e926f351147029ef82015f2ff55da
Source noteuspto-grants-2014_10