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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288031Generated: November 1, 2026

Sodium borohydride → HCID 54100911, compound

https://huagongshe.com/reaction/2288031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54256692HCID 54256692—
SolventMethanolHCID 887—
ProductHCID 54100911HCID 54100911232%

Reaction Steps

To a solution of 16.6 g (39.1 mmol) of 3-ethoxycarbonylmethylidene-1-triphenylmethyl-4-piperidone in 150 ml of methanol, 1.48 g (39.1 mmol) of sodium borohydride were added in portions under ice cooling, followed by stirring at room temperature for 1 hour. After the reaction mixture was concentrated by evaporation under reduced pressure, 50 ml of water and 150 ml of ethyl acetate were added to the concentrate for extraction. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure, whereby 16.8 g (yield: 100%) of 3-ethoxycarbonylmethylidene-4-hydroxypiperidine were obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087379
Source datasetuspto-grants-2000_07
ORD IDord-cd1624441d2a461f9c45a950377fc674
Source noteuspto-grants-2000_07