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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863477Generated: October 31, 2026

Sodium borohydride → HCID 20542033, compound

https://huagongshe.com/reaction/1863477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20542010HCID 20542010—
ReactantHCID 70553603HCID 70553603—
SolventIsopropanolHCID 3776—
ProductHCID 20542033HCID 20542033—

Reaction Steps

A mixture of crude 1,2,3,4-tetrahydro-6,8-dimethoxy-1-oxo-2-naphthaldehyde ethylene acetal obtained from 5.73 g. of 2-hydroxymethylene-6,8-dimethoxy-1-tetralone, and 0.91 g. of sodium borohydride in 25 ml. of 2-propanol was stirred two hours at room temperature. The mixture was cooled and treated with 80 ml. of saturated aqueous ammonium chloride and extracted with ether. The ethereal extracts were washed with saturated aqueous solutions of sodium bicarbonate and sodium chloride, dried over anhydrous magnesium sulfate and evaporated to dryness to give 1,2,3,4-tetrahydro-1-hydroxy-6,8-dimethoxy-2-naphthaldehyde ethylene acetal which was converted directly to 3,4-dihydro-6,8-dimethoxy-2-naphthaldehyde as described hereinabove in Example 154.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04169108
Source datasetuspto-grants-1979_09
ORD IDord-c2dc272900c94d0ea8f7209732c4af83
Source noteuspto-grants-1979_09