Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863214Generated: October 26, 2026

1,3-Dichloro-2-propanol → 1-(1,2-Benzisothiazol-4-yloxy)-3-chloropropan-2-ol

https://huagongshe.com/reaction/1863214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dichloro-2-propanolHCID 7289—
ReactantSodium HydroxideHCID 14798—
ReactantBenzo[d]isothiazol-4-olHCID 135741992—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(1,2-Benzisothiazol-4-yloxy)-3-chloropropan-2-olHCID 20349937—

Reaction Steps

30.0 g of 4-hydroxy-1,2-benzisothiazole are suspended in 26.0 g of 1,3-dichloro-propan-2-ol and a solution of 8.5 g of sodium hydroxide in 60 ml of water is added in the course of 4 hours at 60°-80° C. After reacting for a further four hours at the same temperature, the organic phase is taken up in methylene chloride, dried over magnesium sulfate and evaporated to dryness. The residue left (35 g) is recrystallized from methanol. The 1-(1,2-benzisothiazol-4-yloxy)-3-chloropropan-2-ol thus obtained is identical with the sample prepared as described in (a). Preparation of compounds according to the invention

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168317
Source datasetuspto-grants-1979_09
ORD IDord-085460735fff4d1587f01de72b01bf2b
Source noteuspto-grants-1979_09