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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112010Generated: October 31, 2026

Triethylamine → HCID 86601925, compound

https://huagongshe.com/reaction/2112010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68868795HCID 68868795—
SolventDichloromethaneHCID 6344—
ProductHCID 86601925HCID 8660192595.5%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Methyl 2-({3-[2-(4-hydroxyphenoxy)ethyl]phenoxy}methyl)benzoate (0.096 g, 0.25 mmol) was dissolved in dichloromethane (10 ml) and cooled to −20° C. Triethylamine (0.039 g, 0.38 mmol) was added drop wise and methanesulfonyl chloride (0.032 g, 0.28 mmol) was added drop wise. The ice bath was removed and the mixture was wormed to room temperature. Diethyl ether (5 ml) was added and the precipitate filtered off. The organic phase was washed with two portions of brine (5 ml) and dried (MgSO4). Removing The solvent was removed by evaporation giving 0.109 gram of methyl 2-{[3-(2-{4-[(methylsulfonyl)oxy]phenoxy}-ethyl)phenoxy]methyl}benzoate (yield 94.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521461B2
Source datasetuspto-grants-2009_04
ORD IDord-cd6281af9e7b4edfbb5d84a3d3f3845b
Source noteuspto-grants-2009_04