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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449120Generated: November 3, 2026

Acetic Acid → 7-Amino-4-benzyloxy-1,2-benzisothiazole

https://huagongshe.com/reaction/1449120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
Reactant7-Nitro-4-benzyloxy-1,2-benzisothiazoleHCID 20349942—
CatalystIronHCID 23925—
Solvent1-PropanolHCID 1031—
Product7-Amino-4-benzyloxy-1,2-benzisothiazoleHCID 20349935100%

Reaction Steps

28.6 g of 7-nitro-4-benzyloxy-1,2-benzisothiazole are added in portions to a boiling mixture of 67 ml of water, 30 g of iron powder, 3 ml of glacial acetic acid and 167 ml of n-propanol and the mixture is then refluxed for a further hour. When it has cooled, it is neutralized with concentrated ammonia solution and filtered. The filter residue is washed with methylene chloride and the combined wash solutions are dried over magnesium sulfate and freed from the solvent under reduced pressure. 25.1 g (100% of theory) of 7-amino-4-benzyloxy-1,2-benzisothiazole of melting point 126°-128° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189433
Source datasetuspto-grants-1980_02
ORD IDord-d0ff86413b954b0d97b5004a7967a224
Source noteuspto-grants-1980_02