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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721677Generated: November 1, 2026

Sodium borohydride → HCID 22413568, compound

https://huagongshe.com/reaction/1721677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22413579HCID 22413579—
SolventEthanolHCID 702—
ProductHCID 22413568HCID 2241356897.7%

Reaction Steps

A mixture of 3,4-dihydro-6-(2-quinolylmethoxy)-1(2H)-naphthalenone (1.82 g, 6 mmol), prepared as in step 2, and sodium borohydride (230 mg, 6 mmol) in ethanol (15 mL) was refluxed for 30 minutes. The reaction was allowed to warm to ambient temperature and was then quenched with saturated NH4Cl. Extraction with ethyl acetate and purification on a silica gel column eluting with 9:1 CH2Cl2 -ethyl acetate afforded 1.79 g of 1,2,3,4-tetrahydro-6-(2-quinolylmethoxy)-1-naphthalenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512581
Source datasetuspto-grants-1996_04
ORD IDord-46e7568f9f5948ca864b76f6017de91d
Source noteuspto-grants-1996_04