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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242942Generated: November 2, 2026

1-Naphthol → 1,1-Dimethylethyl 3-[(1-naphthalenyloxy)methyl]-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/2242942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactanttert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 5237175—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 3-[(1-naphthalenyloxy)methyl]-1-pyrrolidinecarboxylateHCID 6741645049.9%

Reaction Steps

A solution of 1.0 g (4.9 mmol) of 1,1-dimethylethyl 3-(hydroxymethyl)-1-pyrrolidinecarboxylate (described in WO 0066557), 0.95 g (6.4 mmol) of 1-naphthalenol and 1.4 g (6.9 mmol) of tri-n-butylphosphine in 40 ml of toluene and 20 ml of tetrahydrofuran, cooled under nitrogen by means of an ice bath, is admixed dropwise with a solution of 1.74 g (6.9 mmol) of ADDP. The reaction mixture is allowed to return to ambient temperature and stirring is continued for 24 hours. The mixture is filtered and the precipitate is rinsed with toluene. It is evaporated to dryness. The residue is taken up in dichloromethane and washed with a 1M aqueous sodium hydroxide solution. It is dried over sodium sulfate and evaporated to dryness. The residue is purified by chromatography on a silica gel column, eluting with dichloromethane and then with a 98/2 mixture of dichloromethane and methanol, to give 0.80 g of product in colorless oil form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674805B2
Source datasetuspto-grants-2010_03
ORD IDord-984e193e0d34494d815f675beac57146
Source noteuspto-grants-2010_03