Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179732Generated: October 30, 2026

Diisopropylethylamine → (1R,3S)-3-(tert-butoxycarbonyl)-2,2-dimethylcyclobutanecarboxylic 2,4,6-trichlorobenzoic anhydride

https://huagongshe.com/reaction/2179732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4,6-Trichlorobenzoyl chlorideHCID 2733703—
Reactant(1R,3S)-3-[(tert-Butoxy)carbonyl]-2,2-dimethylcyclobutane-1-carboxylic acidHCID 21576611—
SolventTetrahydrofuranHCID 8028—
Product(1R,3S)-3-(tert-butoxycarbonyl)-2,2-dimethylcyclobutanecarboxylic 2,4,6-trichlorobenzoic anhydrideHCID 86650109—

Reaction Steps

To a stirred solution of (1R,3S)-3-(tert-butoxycarbonyl)-2,2-dimethylcyclobutanecarboxylic acid (about 0.450 g, 1.97 mmol) and DIPEA (about 1.01 ml, 5.92 mmol) in THF (about 4 ml) and 2,4,6-trichloro benzoyl chloride (0.35 ml, 2.17 mmol) were added at 0° C. and the reaction mixture was allowed to stir at room temperature for about 6 hours, after completion of the reaction (monitored by TLC), the solvent was evaporated and crude product proceeded as such for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067966B2
Source datasetuspto-grants-2015_06
ORD IDord-e5b0dd68cdd448adb4d4f436e53c9182
Source noteuspto-grants-2015_06