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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509899Generated: October 26, 2026

Triethylamine → Benzoic acid, 4-[3-[(methylsulfonyl)oxy]propyl]-, methyl ester

https://huagongshe.com/reaction/509899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 4-(3-hydroxypropyl)benzoateHCID 14425137—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 4-[3-[(methylsulfonyl)oxy]propyl]-, methyl esterHCID 10423370—

Reaction Conditions

Temperature-15 °C

Reaction Steps

4-(3-Hydroxy-propyl)-benzoic acid methyl ester (1.27 g, 6.5 mmol) and triethylamine (1 ml, 7.1 mmol) are dissolved in dichloromethane (30 ml), cooled to −15° C., methanesulfonylchloride (510 μl, 6.5 mmol) is added and stirred at room temperature for 4 h. The reaction mixture is diluted with dichloromethane, washed with potassiumhydrogensulfoate solution and potassiumcarbonate solution, the organic phase is dried over Na2SO4 and concentrated in vacuo. LC (method F): tR=1.88 min; Mass spectrum (ESP): m/z=295 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096548B2
Source datasetuspto-grants-2015_08
ORD IDord-ea01f834f6724491a8a5256947c0a475
Source noteuspto-grants-2015_08