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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398037Generated: October 30, 2026

Hydrochloric Acid → methyl 4-hydroxy-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide

https://huagongshe.com/reaction/2398037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl-2,3-dihydro-3-oxo-1,2-benzisothiazoline-2-acetate 1,1-dioxideHCID 86733499—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl 4-hydroxy-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxideHCID 54676531—

Reaction Conditions

Temperature10 °C

Reaction Steps

In a nitrogen atmosphere, a solution of 30 grams (0.117 moles) of methyl-2,3-dihydro-3-oxo-1,2-benzisothiazoline-2-acetate 1,1-dioxide in 50 ml DMF is added, with stirring, to a suspension of 18.9 grams (0.351 moles) of sodium methoxide in 100 ml DMF over a period of about 5 minutes and the internal temperature is maintained at 15°-30° C. by means of an ice bath. The stirring is continued for 30 minutes at about 30° C. after the completion of the addition. With external cooling, a solution of 35 ml concentrated HCl in 600 ml of water is added, maintaining the internal temperature below 35° C. After this addition, the mixture is cooled to 10° C. and filtered. The filter cake is washed thoroughly with water and the product is dried. Yield is 23.5 grams (78.2%) m.p. 173°-175° C. The total addition and stirring time prior to acidification should be less than 1 hour. For example, if the addition should take 30 minutes the batch should be stirred only an additional 15-20 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024136
Source datasetuspto-grants-1977_05
ORD IDord-bef7748b6729454ebb4975ffef1712e9
Source noteuspto-grants-1977_05