HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398041Generated: October 27, 2026
Methanethiol → Ethyl nitro(1,3-thiazinan-2-ylidene)acetate
https://huagongshe.com/reaction/2398041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Ethyl nitroacetate | HCID 69379 | — |
| Reactant | 4H-1,3-Thiazine | HCID 21989997 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Diethyl ether 2-propanol | HCID 22147583 | — |
| Product | Ethyl nitro(1,3-thiazinan-2-ylidene)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04024138 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-0863cf405b6b4939a1280cb61ef69427 |
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| Source note | uspto-grants-1977_05 |
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