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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515156Generated: October 27, 2026

Sodium Hydroxide → HCID 72187844, compound

https://huagongshe.com/reaction/515156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
ReactantHCID 86699732HCID 86699732—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTetrahydrofuranHCID 8028—
SolventBenzene tetrahydrofuranHCID 22633675—
ProductHCID 72187844HCID 72187844115%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution 2-(ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzamide (0.27 g, 0.88 mmol) in benzene-tetrahydrofuran (1:1) (10 ml) are added tetrabutylammonium hydrogensulfate (0.03 g, 0.09 mmol) and 15% sodium hydroxide solution (8 ml) at RT. 4-Chlorobenzyl bromide (0.083 g, 0.40 mmol) in tetrahydrofuran (1.5 ml) is added and the reaction mixture is slowly heated to 70° C. The reaction mixture is stirred at 70° C. for additional 25 min. After completion of the reaction (monitored by TLC), the organic layer is separated and the aqueous layer is extracted with ethyl acetate (2×20 ml). The organic layer is washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 15% acetone/hexane) to yield N-[(4-chlorophenyl)-methyl]-2-(ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzamide (example 8) (0.20 g, 0.46 mmol, 74%). [M+H]+ 437.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-d14e48719d6a4836a1af24a995cfe2ac
Source noteuspto-grants-2015_08