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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888447Generated: November 1, 2026

Triethylamine → 4-(4-Bromobenzyl)thiomorpholine

https://huagongshe.com/reaction/1888447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThiomorpholineHCID 67164—
Reactant4-Bromobenzyl bromideHCID 68527—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Bromobenzyl)thiomorpholineHCID 785841103.8%

Reaction Steps

A mixture of 4-bromobenzyl bromide (1.0 g, 4.0 mmol), triethylamine (0.84 mL, 6.0 mmol) and thiomorpholine (0.82 mL, 8.0 mmol) in THF (10 mL) was stirred at ambient temperature for 16 h. The solvent was evaporated and the resultant residue diluted with saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate (2×50 mL). The combined organic layer was dried over sodium sulfate, filtered and evaporated to afford the title compound as an off-white solid (1.13 g, quantitative yield). 1H NMR (CDCl3, 300 MHz): 7.46-7.40 (m, 2H), 7.21-7.16 (m, 2H), 3.45 (s, 2H), 3.15-3.09 (m, 1H), 2.76-2.60 (m, 6H), 2.62-2.57 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-f5daac80fd8c4dc3bb8c3f9b8de408ed
Source noteuspto-grants-2013_08