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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485873Generated: October 30, 2026

Sodium borohydride → HCID 13952868, compound

https://huagongshe.com/reaction/485873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20197895HCID 20197895—
SolventEthanolHCID 702—
ProductHCID 13952868HCID 13952868—

Reaction Steps

Sodium borohydride (2.5 g) is added, in small portions, to a stirred solution of 5.0 g of 6,7-dichloro-5-methoxy-2-methylbenzo[b]thiophen-3(2H)-one (5.0 g), in 120 ml of ethanol. Stirring is continued at room temperature for 1 hour and excess solvent is removed under reduced pressure. The residue is triturated with dilute sodium hydroxide solution and extracted 3 times with ether. The combined ether solution is washed thoroughly with water, dried and concentrated. Removal of ether leaves an oily residue which crystallized upon cooling. For analysis, a small sample was washed with pentane and dried at 60° C. to give 6,7-dichloro-2,3-dihydro-3-hydroxy-5-methoxy-2-methylbenzo[b]thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537976
Source datasetuspto-grants-1985_08
ORD IDord-cca494339e3a435ba7ac9e1eb82b22cb
Source noteuspto-grants-1985_08