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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726175Generated: October 30, 2026

Sodium borohydride → HCID 44211738, compound

https://huagongshe.com/reaction/726175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 44211737HCID 44211737—
SolventEthanolHCID 702—
ProductHCID 44211738HCID 44211738—

Reaction Steps

(1-Butylpiperidin-4-ylmethyl)thiochroman-4-one-8-carboxylate (0.064 g, 0.177 mmol)(Example 2-1) was dissolved in ethanol (5 ml) and treated with sodium borohydride (0.007 g, 0.186 mmol) with stirring. After 3 h, the reaction mixture was evaporated under reduced pressure and the residue partitioned between CH2Cl2 and water. The aqueous layer was then extracted with CH2Cl2 and the combined organic extracts were dried (Na2SO4) and evaporated under reduced pressure to give the title compound as a pale yellow oil which was dried in vacuo (0.060 g, 93%) and subsequently converted to the oxalate salt. m.pt 147°-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708174
Source datasetuspto-grants-1998_01
ORD IDord-45d9f804815f4f46ae7d23fb4d4adad0
Source noteuspto-grants-1998_01