Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089024Generated: November 2, 2026

Sodium borohydride → HCID 19961064, compound

https://huagongshe.com/reaction/1089024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Cyano-5,6-dimethoxy-3-phenyl-3,4-dihydronaphthaleneHCID 19961162—
SolventEthanolHCID 702—
ProductHCID 19961064HCID 19961064—

Reaction Steps

Sodium borohydride (6.8 g) was added to a suspension of 6.8 g (23.3 mmol) of 1-cyano-3,4-dihydro-5,6-dimethoxy-3-phenyl naphthalene, from Step 1, in 100 mL of absolute ethanol and the reaction mixture was heated at reflux temperature for 1.5 h. The solvent was evaporated under reduced pressure and the residue was dissolved in ethyl acetate. The ethyl acetate solution was washed with 1N aqueous hydrochloric acid solution, aqueous sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, filtered and concentrated to an oil. The oil was "triturated" with heptane to give 5.63 g (82%) yield of the title compound as a white crystalline solid, m.p. 118°-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963568
Source datasetuspto-grants-1990_10
ORD IDord-7827e6b1d3744490a9dcb0ba45a32e49
Source noteuspto-grants-1990_10