Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681179Generated: November 2, 2026

Water → HCID 10358222, compound

https://huagongshe.com/reaction/1681179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzyl bromideHCID 68021—
Reactant(1-Benzylpiperidin-4-yl)methanolHCID 736802—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10358222HCID 1035822259.2%

Reaction Steps

A suspension of sodium hydride (60% dispersion in oil, 0.76 g, 19 mmol) in anhydrous tetrahydrofuran (38 mL) was stirred at room temperature under a nitrogen atmosphere. A solution of 1-benzyl-4-hydroxymethyl piperidine (3.82 g, 18.6 mmol) was added dropwise. After the addition was completed, the reaction mixture was stirred for 2 h. 4-Fluorobenzyl bromide (2.4 mL, 19 mmol) was added dropwise, then the reaction mixture was stirred for 72 h. Water (50 mL) was added and the resulting mixture was extracted three times with ethyl acetate. Drying over magnesium sulfate, filtration and concentration in vacuo gave an oil. Vacuum distillation (170° C. (Kugelrohr oven), 1.0 Torr) gave a colorless oil (3.45 g, 59% yield): 'H-NMR: 7.34-6.98 (m, 9H), 4.46 (s, 2H), 3.50 (s, 2H), 2.93-2.87 (m, 2H), 2.02-1.59 (m, 5H), 1.39-125 HR-MS Calcd.: 313.1478; Found: 313.1479; (m, 2H); Anal. Calcd.: for C20H24FNO: C,76.65, H,7.72, N,4.47; Found: C,77.27, H,7.69, N,4.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169855
Source datasetuspto-grants-1992_12
ORD IDord-7b6ba86995974316aa5f5feb10734bca
Source noteuspto-grants-1992_12