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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263283Generated: October 31, 2026

Sulfuric Acid → HCID 13343680, compound

https://huagongshe.com/reaction/1263283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantHCID 13343675HCID 13343675—
ReactantHCID 13343703HCID 13343703—
SolventEthanolHCID 702—
ProductHCID 13343680HCID 13343680—

Reaction Steps

8-Chloro-3-(o-chlorophenyl)-5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acid (4d) was prepared from (3d) using the procedure above; the product contained a significant impurity, presumably the countercyclized 5-(3-benzisoxazolyl)-6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acid. The mixture was dissolved in 200 ml. absolute ethanol and treated with 0.5 ml. concentrated sulfuric acid overnight. The solution was then evaporated to dryness, redissolved in ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate, and re-evaporated. Chromatography of the ester on silica gel with chloroform and n-hexane in a 3:1 ratio gave a solid, m.p. 136° C., which was determined by detailed mass spectral analysis to be the desired isomer. Hydrolysis at 60° C. in 25 ml. absolute ethanol and 200 ml. aqueous 1M sodium hydroxide for 20 minutes furnished a white precipitate which was distributed between ethyl acetate and 4.0M aqueous hydrochloric acid, washed with brine, dried over anhydrous magnesium sulfate, and evaporated. Recrystallization from ethyl acetate with n-hexane gave (4d), m.p. 224°-225° C., in 8.1% yield. Analysis (C16H9Cl2NO4) C,H,N,Cl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04456612
Source datasetuspto-grants-1984_06
ORD IDord-21a8a9b7fac94cbebd81309dcb158916
Source noteuspto-grants-1984_06