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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550036Generated: October 31, 2026

Potassium Carbonate → Benzyl(S)-2-((2'-cyanobiphenyl-4-ylmethyl)pentanoylamino)-3-methylbutyrate

https://huagongshe.com/reaction/550036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantValeryl chlorideHCID 61186—
ReactantHCID 44252740HCID 44252740—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzyl(S)-2-((2'-cyanobiphenyl-4-ylmethyl)pentanoylamino)-3-methylbutyrateHCID 46912012—

Reaction Steps

A mixture of potassium carbonate (95.3 g) and de-mineralized water (100 ml) was stirred for 10 to 15 minutes to dissolve the solid. The temperature of the mixture was maintained at 25° to 30° C. and dichloromethane (300 ml) was added to the mixture. (S)—N-[(2′-Cyanobiphenyl-4-yl)methyl]-(L)-valine benzyl ester hydrochloride (100 g) and tetrabutyl ammonium bromide (10.0 g) were added to the mixture. The reaction mixture was cooled to −10° to −8° C. and valeryl chloride (36.1 g) was added at −10° to −5° C. The reaction mixture was stirred for 60 to 90 minutes at 0° to 5° C. After the completion of the reaction, the temperature was raised to 25° to 30° C. De-mineralized water (200 ml) was added to the reaction mixture and the mixture was stirred for 1 hour at 25° to 30° C. The two phases were separated and the organic layer was washed with de-mineralized water (200 ml). The organic layer was concentrated at 40° to 45° C. to obtain a residual liquid containing the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943794B2
Source datasetuspto-grants-2011_05
ORD IDord-16ff3ddfe4f745d4851d7da5322ae0a0
Source noteuspto-grants-2011_05