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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635232Generated: October 27, 2026

Water → Methyl 4-[(1-Boc-piperidin-4-ylidene)methyl]benzoate

https://huagongshe.com/reaction/635232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-(Dimethoxy-phosphorylmethyl)-benzoic acid methyl esterHCID 10801170—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[(1-Boc-piperidin-4-ylidene)methyl]benzoateHCID 1061649935%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The crude product (compound 48) was dissolved in dry THF (200 mL) under N2 and cooled to −78° C. Lithium diisopropylamide (32.7 mL 1.5 M in hexanes, 49 mmol) was added dropwise. The solution was allowed to warm to room temperature. A solution of compound 46 (9.76 g, 49 mmol in 100 mL dry THF) was added to the reaction dropwise and was stirred under N2 for 12 hrs. Water (300 mL) and ethyl acetate (300 mL) were added to the reaction mixture and extracted. The aqueous phase was washed with ethyl acetate (2×300 mL). The combined ethyl acetate was dried over MgSO4 and evaporated to give a crude product, which was purified by silica gel chromatography (0-33% ethyl acetate in hexanes) to provide compound 49 as a white solid (5.64 g, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187792B1
Source datasetuspto-grants-2001_02
ORD IDord-4e7d1400b1eb4207a9eb2947d00bd81a
Source noteuspto-grants-2001_02