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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657695Generated: October 27, 2026

2-Nitro-1-phenylethanone → 2-nitro-1-phenyl-2-(tetrahydro-2H-1,3-thiazin-2-ylidene)ethanone

https://huagongshe.com/reaction/1657695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-1-phenylethanoneHCID 94833—
Reactant2-(methylsulfanyl)-5,6-dihydro-4H-1,3-thiazineHCID 2782081—
CatalystZincchlorideHCID 3007855—
Product2-nitro-1-phenyl-2-(tetrahydro-2H-1,3-thiazin-2-ylidene)ethanoneHCID 73179523—

Reaction Steps

A mixture of 3.3 g of 2-nitroacetophenone and 2.94 g of 2-(methylthio)-5,6-dihydro-4H-1,3-thiazine was heated to 115° and 100 milligrams of zinc chloride was added. Heating and stirring was continued at 115°-120° for 2.5 hours. After cooling, the mixture was filtered (with the aid of ethyl acetate) through a short column of florosil to give an amber oil. The oil was chromatographed on silica gel using dry-column technique and a 1:1:2 mixture of tetrahydrofuran/ethyl acetate/hexane for development to give 1 as a salmon-colored solid, m.p.: 137°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962225
Source datasetuspto-grants-1976_06
ORD IDord-c121f869ad254e72aa5ed30b52d0f3d5
Source noteuspto-grants-1976_06