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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49328Generated: October 26, 2026

Triethylamine → 5-(2-Ethyl-[1,3]dioxolan-2-yl)-2-thienylmethyl methanesulphonate

https://huagongshe.com/reaction/49328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant[5-(2-Ethyl-[1,3]dioxolan-2-yl)-2-thienyl]methanolHCID 17934796—
SolventDichloromethaneHCID 6344—
Product5-(2-Ethyl-[1,3]dioxolan-2-yl)-2-thienylmethyl methanesulphonateHCID 20636301—

Reaction Conditions

Temperature0 °C

Reaction Steps

9.25 g (43.2 mmol) of [5-(2-ethyl-[1,3]dioxolan-2-yl)-2-thienyl]methanol are dissolved in 500 mL of dichloromethane and cooled to 0° C. 9.0 mL (64.7 mmol) of triethylamine are added, followed by 3.5 mL of methylsulphonyl chloride (45.3 mmol). After stirring for 1 hour, the reaction medium is treated with ammonium chloride solution and extracted with dichloromethane. The organic phases are combined, dried and concentrated under reduced pressure. A brown oil is obtained (m=9.28 g; Y=75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706725B1
Source datasetuspto-grants-2004_03
ORD IDord-1df85117b94e458c8d44dd2cbc29df2c
Source noteuspto-grants-2004_03