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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291162Generated: October 30, 2026

Triethylamine → HCID 765448, compound

https://huagongshe.com/reaction/1291162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-(bromomethyl)-3-nitro-HCID 77568—
ReactantPiperidin-4-olHCID 79341—
SolventDimethylformamideHCID 6228—
ProductHCID 765448HCID 76544858%

Reaction Steps

1.41 g (0.01389 mol) of 4-hydroxypiperidine were dissolved in 60 ml of dimethylformamide and cooled to 0°. 3.0 g (0.01389 mol) of 3-nitrobenzyl bromide and 4.3 ml (0.03056 mol) of triethylamine were added under argon and the mixture was left to come to room temperature. It was stirred for 16 hrs., the solvent was distilled off and the residue was taken up in dichloromethane. The organic phase was washed with water and saturated sodium chloride solution, dried over magnesium sulfate and concentrated and the residue was chromatographed on silica gel with dichloromethane/methanol (19:1) as the eluent. 1.9 g (58%) of 1-(3-nitro-benzyl)-piperidin-4-ol were obtained as a yellow oil. MS: me/e=237 (C12H17N2O3+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-1ba0eaf07b644a3ebed16a47dd5df114
Source noteuspto-grants-1998_05