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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198446Generated: October 25, 2026

Water → 3-(4-chlorophenyl)-1-(3-chloropropyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one

https://huagongshe.com/reaction/1198446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-oneHCID 18984440—
SolventDimethyl SulfoxideHCID 679—
Product3-(4-chlorophenyl)-1-(3-chloropropyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-oneHCID 5402738565.1%

Reaction Steps

To a solution of 3-(4-chlorophenyl)-1H-naphtho-[2,1-b][1,4]thiazin-2(3H)-one (10.0 g) and 96% sodium hydroxide (1.96 g) in dimethylsulfoxide (150 ml) is added 1-bromo-3-chloropropane (6.78 g) under ice cooling, and the mixture is stirred at room temperature overnight. The reaction mixture is poured into water, and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed and distilled to remove the solvent. The residue is purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=5:1) and further is recrystallized from methanol to give 3-(4-chlorophenyl)-1-(3-chloropropyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3-H)-one (8.04 g). M.p. 110°-112.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281592
Source datasetuspto-grants-1994_01
ORD IDord-4c19dc03a62c425cbe2ed86f81faf68d
Source noteuspto-grants-1994_01