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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353425Generated: November 2, 2026

Acetic Anhydride → HCID 73553252, compound

https://huagongshe.com/reaction/2353425

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., sodium bis(trimethylsilyl)amide (4.18 mL, 1.0 M in tetrahydrofuran) was added. 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 numberUS07750034B2
Source datasetuspto-grants-2010_07
ORD IDord-07a7c3b9263a4264bed5db17caec3e38
Source noteuspto-grants-2010_07