Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241563Generated: October 29, 2026

Acetic Anhydride → HCID 73553252, compound

https://huagongshe.com/reaction/241563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
ProductHCID 73553252HCID 73553252—

Reaction Steps

To a solution of tert-butyl 3-oxopyrrolidine-1-carboxylate (370 mg) in tetrahydrofuran (20 mL) at −78° C. was added sodium bis(trimethylsilyl)amide (4.18 mL, 1.0M in tetrahydrofuran). The reaction mixture was stirred for 1.5 h, then treated with acetic anhydride (0.21 mL) and stirred at room temperature for 20 min. The reaction mixture was quenched by the dropwise addition of water and concentrated under vacuum. To the basic residue, ethyl acetate (50 mL) and saturated aqueous sodium bicarbonate solution (30 mL) with an equal volume of water were added. The aqueous layer was separated, acidified by careful addition of hydrochloric acid to pH 3 and extracted with ethyl acetate (75 mL). The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated to yield desired product which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653059B2
Source datasetuspto-grants-2014_02
ORD IDord-7e9477ac185141e8824536d35d09487a
Source noteuspto-grants-2014_02