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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989458Generated: October 30, 2026

Hydrochloric Acid → HCID 12098836, compound

https://huagongshe.com/reaction/989458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
ReactantN,N-Dibenzyl-L-phenylalanineHCID 10980880—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 12098836HCID 1209883699%

Reaction Steps

Dehydrated tetrahydrofuran (15 ml) was cooled to −78° C. 1.53 M solution (6.5 ml) of n-butyllithium in hexane and then a solution of methylene chloride (0.8 ml) in dehydrated tetrahydrofuran (5 ml) were added thereto, and they were stirred for 10 minutes. A solution of benzyl ester (2.18 g) of N,N-dibenzyl-L-phenylalanine in dehydrated tetrahydrofuran (7 ml) was added to the obtained mixture, and they were stirred for 1 hour. 2 N hydrochloric acid (15 ml) and water (15 ml) were added to the reaction mixture to terminate the reaction. The temperature was elevated to room temperature. After the addition of water followed by the extraction with ethyl acetate, the obtained solutions in ethyl acetate were combined together and dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered out. The solvent was evaporated under reduced pressure to obtain the intended (3S)-1,1-dichloro-3-dibenzylamino-4-phenyl-2-butanone (2.04 g) in a yield of 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06639094B2
Source datasetuspto-grants-2003_10
ORD IDord-f2421b823cac4d0cb2570336223206b1
Source noteuspto-grants-2003_10