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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072489Generated: October 30, 2026

Sodium borohydride → HCID 68120077, compound

https://huagongshe.com/reaction/2072489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 131710914HCID 131710914—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 68120077HCID 6812007782.7%

Reaction Steps

8-[(6-(Trifluoromethyl)-1,2,3,4-tetrahydro-1-oxo-2-naphthal-enyl)methyl]-1-phenyl-1,3,8,-triazaspiro[4.5]decan-4-one, hydrochloride (1:1) (0.65 g, see example 184) is slurried in methanol (10 ml) and, with cooling, treated with a solution of sodium borohydride (0.27 g) in water (2 ml). The resulting mixture is stirred at room temperature under nitrogen for 16 hours, diluted with water (10 ml), and extracted with methylene chloride. Concentration of the dried organic solution followed by trituration with absolute ethanol yields the free base of the title alcohol as a tan powder (0.5 g), melting point 238°-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04051248
Source datasetuspto-grants-1977_09
ORD IDord-edbde72a00c14ebca987a4dd3d9bcde7
Source noteuspto-grants-1977_09