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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462632Generated: October 30, 2026

Sodium borohydride → HCID 13264151, compound

https://huagongshe.com/reaction/462632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13264142HCID 13264142—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13264151HCID 1326415187%

Reaction Steps

2.0 g of methyl rac-1',2',3',4'-tetrahydro-2'-hydroxy-5',8'-dimethoxyspiro[1,3-dithiolane-2,4'-naphthalene]-2'-carboxylate, prepared as described in Example 4(iv), were dissolved in 200 ml of dry tetrahydrofuran and 2.0 g of sodium borohydride were added to the solution. The resulting mixture was stirred at room temperature under nitrogen for 20 hours. The solvent was removed by evaporation and 100 ml of 10% ammonium chloride solution were added. The mixture was extracted with three 30 ml portions of ethyl acetate. The extracts were dried and evaporated to give a colourless oil. Crystallization of this oil from ethyl acetate/petroleum ether gave 1.6 g (87%) of rac-1',2',3',4'-tetrahydro-3'-hydroxy-3'-hydroxymethyl-5',8'-dimethoxyspiro[1,3-dithiolane-2,1'-naphthalene] of melting point 132.5°-133.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515969
Source datasetuspto-grants-1985_05
ORD IDord-63edb4f893a84deebed480f6608ccc60
Source noteuspto-grants-1985_05