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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084420Generated: November 1, 2026

Chlorosuccinimide → HCID 15158732, compound

https://huagongshe.com/reaction/1084420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantLithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
ReactantHCID 23672793HCID 23672793—
ReactantHCID 23694644HCID 23694644—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventCyclohexaneHCID 8078—
ProductHCID 15158732HCID 15158732—

Reaction Steps

To a solution of the mixture obtained in Step 2 (100 g) in anhydrous ether (430 ml) was added dropwise 1.5 M lithium diisopropylamide mono(tetrahydrofuran) in cyclohexane (430 ml) under nitrogen atmosphere at -70° C. After stirring for 30 minutes, into the solution was bubbled sulfur dioxide for 1 hour with stirring at -60° C. Then the solution was stirred for 3 hours at room temperature and the formed precipitate was separated by filtration to give a mixture of lithium 4-bromobenzo[b]furan-2-sulfinate and lithium 6-bromobenzo[b]furan-2-sulfinate. To the suspension of the products in dichloromethane (2 1) was added N-chlorosuccinimide (96 g) at -50° C. and stirred for 3 hours under ice-cooling. Insoluble matters were filtered off and dichloromethane was removed in vacuo and the residue was purified by silica gel column chromatography to give 14.1 g of the objective compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004751
Source datasetuspto-grants-1991_04
ORD IDord-fdd6d00775104e9994397231ca007a55
Source noteuspto-grants-1991_04