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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187639Generated: October 29, 2026

Borohydride → HCID 18476198, compound

https://huagongshe.com/reaction/2187639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
ReactantHCID 54000908HCID 54000908—
SolventMethanolHCID 887—
ProductHCID 18476198HCID 1847619848.2%

Reaction Steps

To a solution of 0.36 g (1.36 mmol) of 5-chloro-2-(hepten-1-yl)benzo[b]thiophene in 50 ml methanol were added 5 g (15 mmol) of borohydride exchange resin and 375 mg (1.51 mmol) Ni(II)acetate tetrahydrate, and the mixture was refluxed for 1 h. It was cooled to room temperature and the resin removed by filtration. The resin was heated twice with 50 ml methanol, and the combined filtrates were concentrated under reduced pressure. The residue was eluted through a column of silica gel with hexane, and the eluant was evaporated to give 175 mg (48%) of the title compound as a colorless resinous oil; MS 266 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410562B1
Source datasetuspto-grants-2002_06
ORD IDord-59ec33cfe79e4d87b97322d584825494
Source noteuspto-grants-2002_06