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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258679Generated: October 26, 2026

Methanethiol → Ethyl nitro(1,3-thiazinan-2-ylidene)acetate

https://huagongshe.com/reaction/258679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantEthyl nitroacetateHCID 69379—
Reactant2-(methylsulfanyl)-5,6-dihydro-4H-1,3-thiazineHCID 2782081—
CatalystZincchlorideHCID 3007855—
SolventDiethyl ether 2-propanolHCID 22147583—
ProductEthyl nitro(1,3-thiazinan-2-ylidene)acetateHCID 71443329—

Reaction Steps

To a mixture of 235 g of 5,6-dihydro-2-(methylthio)-4H-1,3-thiazine and 2 g of zinc chloride at approximately 115° in a nitrogen atmosphere, 263 g of ethyl nitroacetate was added dropwise over a 1.5 hour period. The mixture was held at 110°-120°. When evolution of methyl mercaptan ceased after 45 minutes further stirring of the heated mixture, 1 g of zinc chloride was added and the mixture was stirred at about 115° for 1.25 hours. An additional 1 g of zinc chloride then was added and stirring of the mixture at about 115° was continued for 1.5 hours. The mixture then was poured into a cooled solution of 2/1 ether/isopropyl alcohol mixture. The crystallized product was collected, washed with ether and dried under reduced pressure to leave a tan solid, m.p. 100°-102°, which on recrystallization from methanol gave ethyl nitro(tetrahydro-2H-1,3-thiazin-2-ylidene)acetate (1A) as a pale yellow solid, m.p. 105°-106°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034091
Source datasetuspto-grants-1977_07
ORD IDord-fff921be074a44da950e6193567f2c95
Source noteuspto-grants-1977_07