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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424570Generated: November 2, 2026

Hydrochloric Acid → HCID 58137305, compound

https://huagongshe.com/reaction/1424570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantBenzyl BromideHCID 7498—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 1-benzoyl-3-piperidinecarboxylateHCID 3784394—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58137305HCID 5813730591%

Reaction Steps

To a solution of ethyl 1-benzoylpiperidine-3-carboxylate (9.22 g, 35 mmol) in dry THF (55 mL) at −78° C. was added dropwise LDA (39 mmol, 1.1 eq) in 45 mL of dry THF. After addition, the reaction was stirred for 1 h. Then benzyl bromide (6.54 g, 39 mmol, 1.1 eq) was added dropwise under the an atmosphere of N2. The reaction was stirred for another 3 h. The solution was added dropwise 5% HCl at 0° C. and concentrated. The aqueous residue was extracted with CH2Cl2. The combined organic extracts were dried over anhydrous Na2SO4 and evaporated to afford ethyl 1-benzoyl-3-benzylpiperidine-3-carboxylate (11.16 g, 91%). 1H NMR (CD3OD, 400 MHz): δ=1.30 (t, 3H), 1.50˜1.55 (m, H), 2.75 (m, 2H), 3.65 (m, 4H), 4.09 (m, 2H), 7.08 (m, 2H), 7.22 (m, 3H), 7.48 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927715B2
Source datasetuspto-grants-2015_01
ORD IDord-1a02335a08b04c5491a5be22aa2dc281
Source noteuspto-grants-2015_01