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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027135Generated: October 30, 2026

Ammonium Chloride → tert-Butyl 1-methyl-1-hydroxyspiro[indane-3,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/1027135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylateHCID 18673579—
ReactantHCID 178420676HCID 178420676—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 1-methyl-1-hydroxyspiro[indane-3,4'-piperidine]-1'-carboxylateHCID 6708292866.2%

Reaction Steps

tert-Butyl 1-oxospiro[indane-3,4′-piperidine]-1′-carboxylate (0.202 g, 0.671 mmol) was dissolved in THF (3 mL), 3 mmol/L methylmagnesium chloride-THF solution (0.450 mL, 1.34 mmol) was added under ice-cooling, and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added dropwise to the reaction mixture, and the mixture was extracted several times with ethyl acetate. The combined organic layers were dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to give the title compound (0.141 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729264B2
Source datasetuspto-grants-2014_05
ORD IDord-f2a3572f76904e478cfe487f894fec4b
Source noteuspto-grants-2014_05