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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182687Generated: November 2, 2026

Benzoyl chloride → HCID 71282812, compound

https://huagongshe.com/reaction/1182687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71282812HCID 71282812—

Reaction Conditions

Temperature115 °C

Reaction Steps

Et3N (0.5 mL) was added into a solution of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (0.2 g) and benzoyl chloride (0.1 mL) in THF (10 mL). The mixture was heated to 115° C. for 24 hours. The reaction was quenched with water (10 mL). The aqueous layer was extracted with EtOAc (3×10 mL). The combined organic phase was dried over MgSO4 and concentrated to give a residue which was purified by silica gel chromatography to give tert-butyl 7-benzoyl-2,7-diazaspiro[4.4]nonane-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664213B2
Source datasetuspto-grants-2014_03
ORD IDord-846643860ba44fb9b03aab34c35e7fd8
Source noteuspto-grants-2014_03