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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431809Generated: November 1, 2026

Diisopropylethylamine → (2S,4S)-1-tert-butyl 2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl) 4-methylpyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1431809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(4S)-1-(tert-Butoxycarbonyl)-4-methyl-L-prolineHCID 26596883—
Reactant9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-oneHCID 69673292—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(2S,4S)-1-tert-butyl 2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl) 4-methylpyrrolidine-1,2-dicarboxylateHCID 6768213870.5%

Reaction Steps

To a solution of 9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (1.32 g, 3.63 mmol) in MeCN (40 mL) was added (2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic acid (1.0 g, 4.36 mmol) and DIPEA (0.7 mL, 3.99 mmol). After stirring for 18 h, the solution was diluted with EtOAc and washed successively with saturated aqueous NaHCO3 and brine. The organics were dried over MgSO4, filtered and concentrated under reduced pressure. The crude residue was purified by silica column chromatography (10% to 40% EtOAc/hexanes) to afford (2S,4S)-1-tert-butyl 2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl) 4-methylpyrrolidine-1,2-dicarboxylate (1.31 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940718B2
Source datasetuspto-grants-2015_01
ORD IDord-58414e8f5d6f48dd921628574ef36576
Source noteuspto-grants-2015_01