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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888448Generated: November 1, 2026

Triethylamine → 4-(4-Bromo-benzyl)-thiomorpholine 1,1-dioxide

https://huagongshe.com/reaction/1888448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Bromobenzyl bromideHCID 68527—
ReactantThiomorpholine 1,1-dioxideHCID 6484228—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Bromo-benzyl)-thiomorpholine 1,1-dioxideHCID 5232546874%

Reaction Steps

A mixture of 4-bromobenzyl bromide (1.0 g, 4.0 mmol), triethylamine (0.84 mL, 6.0 mmol) and thiomorpholine 1,1-dioxide (1.09 g, 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 (0.90 g, 74%). 1H NMR (CDCl3, 300 MHz): 7.50-7.44 (m, 2H), 7.22-7.16 (m, 2H), 3.60 (s, 2H), 3.09-3.02 (m, 4H), 3.00-2.94 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-d3b06d20a9744f978f47eb146149551b
Source noteuspto-grants-2013_08