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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987173Generated: October 31, 2026

4-Chloroaniline → 1-(1,1-Dimethylethyl) 3-ethyl (3R,4R)-4-[[(4-chlorophenyl)amino]carbonyl]-1,3-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/1987173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 34180170HCID 34180170—
SolventAcetonitrileHCID 6342—
Product1-(1,1-Dimethylethyl) 3-ethyl (3R,4R)-4-[[(4-chlorophenyl)amino]carbonyl]-1,3-pyrrolidinedicarboxylateHCID 69047627—

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 7a (4.91 g; 17.1 mmol) is suspended in acetonitrile (25 ml) and N,N-diisopropyl ethyl amin (3.58 ml; 20.5 mmol) is added at 0° C. Bis(2-oxo-3-oxazolidinyl) phosphinic chloride BOP-Cl (5.22 g; 20.5 mmol) is added as a solid and after stirring for 30 min at 0° C. 4-chloroaniline (2.18 g; 17.1 mmol) is added to the reaction mixture. The mixture is stirred for 2 h at 0° C., evaporated to dryness and dissolved in ethyl acetate (ml). The organic phase is washed with 0.1 N HCl (2×ml), with saturated aquous Na2CO3 solution, water and brine and dried over Na2SO4. The organic phase is filtered and the filtrate is evaporated to dryness. The crude product is purified by silica gel chromatography. Yield: 4.7 g (69.3%), ESI-MS: m/z=395 [M−H]−, Cl-pattern

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550487B2
Source datasetuspto-grants-2009_06
ORD IDord-4d580022d8974e95be7cd62de4e41042
Source noteuspto-grants-2009_06