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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245959Generated: October 26, 2026

Carbon Dioxide → 1,3-Benzothiazol-6-ylmethyl methanesulfonate

https://huagongshe.com/reaction/2245959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-(Hydroxymethyl)benzothiazoleHCID 17860385—
SolventDichloromethaneHCID 6344—
SolventEthylene glycol waterHCID 20437942—
Product1,3-Benzothiazol-6-ylmethyl methanesulfonateHCID 59216292—

Reaction Steps

1,3-benzothiazol-6-ylmethanol (1.56 g, 0.00944 mol) and N,N-diisopropylethylamine (2.47 mL, 0.0142 mol) were stirred in methylene chloride (16 mL). The reaction mixture was cooled in an ethylene glycol/water (4/1)/dry ice bath. To the solution was added dropwise a solution of methanesulfonyl chloride (1.10 mL, 0.0142 mol) in DCM (2 mL). After 30 min the reaction mixture was quenched by adding water, and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give the desired product which was directly used in the next step without purification. LCMC: (M+H)+=244.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683060B2
Source datasetuspto-grants-2010_03
ORD IDord-7206752730114ca78d57f3ef611ce5cb
Source noteuspto-grants-2010_03