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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788279Generated: November 4, 2026

Methanol → HCID 86596808, compound

https://huagongshe.com/reaction/1788279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantTert-butyl 4-(4-bromophenyl)-4-cyanopiperidine-1-carboxylateHCID 49760269—
SolventDichloromethaneHCID 6344—
ProductHCID 86596808HCID 86596808—

Reaction Steps

To a solution of 4-(4-bromo-phenyl)-4-cyano-piperidine-1-carboxylic acid tert-butyl ester from Step 2 (5.67 g, 15.57 mmol, 1 eq) in 60 mL of dichloromethane was add a solution of DIBAL-H (1M in toluene, 23.36 mL, 23.36 mmol, 1.5 eq) in a drop-wise fashion. The resulting mixture was stirred at room temperature for 20 h and then 15 mL of methanol was added carefully. The mixture was stirred for 0.25 h and a precipitate formed. The resulting mixture was filtered through Celite and the salts were washed several times with ethyl acetate. The filtrate was adsorbed onto silica gel and purified by flash column chromatography eluting with a gradient of 5-20% ethyl acetate in hexane to give 1.78 g of 4-(4-bromo-phenyl)-4-(2-oxo-ethyl)-piperidine-1-carboxylic acid tert-butyl ester and 1.54 g of recovered starting material. 1H NMR (300 MHz, CDCl3): δ 9.35 (s, 1H), 7.50-7.46 (d, 2H), 7.15-7.10 (d, 2H), 3.82 (br. s, 2H), 3.11-3.04 (t, 2H), 2.35-2.28 (dt, 2H), 1.90 (br. s, 2H), 1.42 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511146B2
Source datasetuspto-grants-2009_03
ORD IDord-26a28e9c09a047ae98dac8af6f50f05b
Source noteuspto-grants-2009_03