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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037607Generated: October 28, 2026

Hydrochloric Acid → HCID 57577277, compound

https://huagongshe.com/reaction/1037607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropanamide, N-(4-chlorophenyl)-2,2-dimethyl-HCID 182511—
ReactantHCID 58046560HCID 58046560—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 57577277HCID 5757727744.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of n-buthyllithium in hexane (47.0 ml of a 1.6M solution) was added dropwise to a solution of N-(4-chloro-phenyl)-2,2-dimethyl-propionamide (6.35 g) in dry THF (100 ml) at −5° C. under a N2 atmosphere over 15 min. The resulting solution was stirred at 0° C. for 2 hours, and then a solution of 1-[(E)-3-(4-chloro-phenyl)-allyl]-piperidin-4-one (7.49 g) in THF (15 ml) was added dropewise to the above solution of the dianion at 0° C. over a 1 hour period. The reaction mixture was stirred for 2 hours at 0° C. and then overnight at r.t. The solution was then poured into ice water, made acidic with conc. HCl and extracted with ethyl acetate. The water layer was made basic and extracted three times with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was subjected to silica gel chromatography (hexane:ethyl acetate:triethyl amine 49:49:2) to afford the title product (6.2 g). M.p. 177-179° C.; Retention Time HPLC 2.19 min; MS (ES+) 461 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546569B2
Source datasetuspto-grants-2013_10
ORD IDord-5d217a6aecc44991b18ccdb09a8d2daf
Source noteuspto-grants-2013_10