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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912737Generated: November 1, 2026

1-Naphthol → HCID 67416540, compound

https://huagongshe.com/reaction/912737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67416540HCID 67416540100.5%

Reaction Steps

A solution of 5.0 g (23.2 mmol) of 1,1-dimethylethyl 4-(hydroxymethyl)-1-piperidine-carboxylate, 4.3 g (29.8 mmol) of 1-naphthalenol and 7.82 g (29.8 mmol) of triphenylphosphine in 120 ml of tetrahydrofuran, cooled under nitrogen by means of an ice bath, is admixed dropwise with a solution of 6.03 g (29.8 mmol) of diisopropyl azodicarboxylate. The reaction mixture is allowed to return to ambient temperature and stirring is continued overnight. 2 ml of methanol are added and then the mixture is evaporated to dryness. The residue is taken up in 200 ml of dichloromethane and washed in succession with a 10% aqueous potassium hydrogen sulfate solution, water and a 1M aqueous solution of sodium hydroxide. The system is dried over sodium sulfate and evaporated to dryness. The product is purified by chromatography on silica gel, eluting with an 80/20 then 70/30 and 50/50 mixture of cyclohexane and dichloromethane, to give 7.96 g of product in oil form, which solidifies.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026258B2
Source datasetuspto-grants-2011_09
ORD IDord-ced957fac1ec4545a0bec6c19ab807e8
Source noteuspto-grants-2011_09