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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060237Generated: October 31, 2026

Hydrochloric Acid → 1-(4-Methoxy-benzoyl)-pyrrolidine-3,3-dicarboxylic acid ethyl ester

https://huagongshe.com/reaction/2060237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1-(4-Methoxy-benzoyl)-pyrrolidine-3,3-dicarboxylic acid diethyl esterHCID 59322227—
SolventAcetonitrileHCID 6342—
Product1-(4-Methoxy-benzoyl)-pyrrolidine-3,3-dicarboxylic acid ethyl esterHCID 5932222453.4%

Reaction Conditions

Temperature30 °C

Reaction Steps

1-(4-Methoxy-benzoyl)-pyrrolidine-3,3-dicarboxylic acid diethyl ester (679.9 g, 1.95 mol) (see Preparation 7) in acetonitrile (1000 mL) was added to pH 7 buffer solution (10 L, 0.1M potassium phosphate) then Savinase 16T Type W enzyme (3200 g) was added and the resulting slurry was heated to 30° C. The pH of the reaction mixture was kept at 8.5 using a pH stat (TIM856 Titration Manager) and stirred for 6 days. Water (6 L) and ethyl acetate (12 L) was added to the reaction mixture then acidified to pH1 using 2M HCl aqueous solution (6 L). This was filtered through Arbocel™ and the organic layer was separated, washed with water (5 L) then extracted with 0.5M NaOH aqueous solution (7 L). The aqueous phase was acidified using 2M HCl aqueous solution (5 L) and extracted with ethyl acetate (6.5 L). The organic phase was concentrated under reduced pressure to afford the title compound as an orange oil (334.3 g, 53%). (92.9:7.1 ratio of isomers)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278343B2
Source datasetuspto-grants-2012_10
ORD IDord-96a25d6072234f0bbeea1697053899f0
Source noteuspto-grants-2012_10