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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515143Generated: October 26, 2026

Sodium Hydroxide → HCID 72187789, compound

https://huagongshe.com/reaction/515143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Fluorobenzyl bromideHCID 68007—
Reactant2-Ethylsulfanyl-6-methyl-4-morpholin-4-yl-benzamideHCID 86699724—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventBenzene tetrahydrofuranHCID 22633675—
ProductHCID 72187789HCID 7218778916%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-ethylsulfanyl-6-methyl-4-morpholin-4-yl-benzamide (0.26 g, 0.92 mmol) in benzene-tetrahydrofuran (1:1) (20 ml) are added tetrabutylammonium hydrogensulfate (0.031 g, 0.091 mmol) and 50% sodium hydroxide solution (8 ml) at RT. The reaction mixture is heated to 80° C. and 3-fluorobenzyl bromide (0.14 ml of a 2M solution in benzene, 0.28 mmol) is added. The reaction mixture is stirred at 80° C. for 15 min. After completion of the reaction (monitored by TLC), the reaction mixture is diluted with water (15 ml) and extracted with ethyl acetate (15×3 ml). The organic layer is washed with water (20 ml), brine (15 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 25% ethyl acetate/hexane) to yield 2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-6-methyl-4-morpholin-4-yl-benzamide (example 1) (0.06 g, 0.15 mmol, 16%). [M+H]+ 389.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-feb3e339a00a4bd58b1d2ba57e451550
Source noteuspto-grants-2015_08