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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267108Generated: November 1, 2026

Methanol → HCID 59600599, compound

https://huagongshe.com/reaction/2267108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59600612HCID 59600612—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59600599HCID 59600599—

Reaction Steps

A solution of 2H-spiro[naphthalene-1,4′-piperidine]-4-carbonitrile (A4) (66 mg, 0.3 mmol), 3,3-dimethylbutanal (46 mg, 0.46 mmol) in 1,2-dichloroethane (5 ml) was stirred at 40° C. for 2 h. To the solution was added sodium triactoxyborohydride and the resulting mixture was stirred overnight, followed by treatment of MeOH (1 ml). Evaporation and the residue was dissolved in MeOH (2 ml) and purified by reverse phase C-18 HPLC to give 1′-(3,3-dimethylbutyl)-2H-spiro[naphthalene-1,4′-piperidine]-4-carbonitrile (Compound No. 51). LC-MS: m/e=309.1 (M+H). Rt=1.92 min. 1H-NMR (500 MHz, DMSO-d6): 9.03 (br. s, 1H), 7.49-7.40 (m, 4H), 7.12 (t, 1H), 3.45 (d, 2H), 3.22-3.11 (m, 4H), 2.78 (d, 2H), 2.03 (td, 2H), 1.88 (d, 2H), 1.58-1.54 (m, 2H), 0.92 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858790B2
Source datasetuspto-grants-2010_12
ORD IDord-ea7cb14b534847a1bacefd5a9ccfd406
Source noteuspto-grants-2010_12