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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404096Generated: October 31, 2026

Toluene → Methyl 6-(spiro[5.5]undecan-3-yloxy)-2-naphthoate

https://huagongshe.com/reaction/2404096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantMethyl 6-hydroxy-2-naphthoateHCID 390995—
ReactantSpiro[5.5]undecan-3-olHCID 66926515—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-(spiro[5.5]undecan-3-yloxy)-2-naphthoateHCID 66926514—

Reaction Steps

A mixture of spiro[5.5]undecan-3-ol (0.999 g, 0.00593 mol), 6-hydroxy-naphthalene-2-carboxylic acid methyl ester (1.00 g, 0.00494 mol) and triphenylphosphine (1.56 g, 0.00593 mol) in toluene (10 mL, 0.1 mol) was heated to reflux. Diisopropyl azodicarboxylate (1.17 mL, 0.00593 mol) was then added dropwise and the resulting mixture was refluxed for 6 hours. The mixture was then diluted with dichloromethane and subjected to chromatographic purification with ethyl acetate:hexane (0:100 to 40:60) to give methyl 6-(spiro[5.5]undecan-3-yloxy)-2-naphthoate as a white solid. (1.09 g, 62%). 1H NMR (400 MHz, CDCl3) δ 8.52 (s, 1H), 8.01 (dd, J=8.7, 1.7 Hz, 1H), 7.84 (d, J=9.6 Hz, 1H), 7.72 (d, J=8.7 Hz, 1H), 7.17 (m, 2H), 4.45 (m, 1H), 3.97 (s, 3H), 1.93-1.28 (m, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802659B2
Source datasetuspto-grants-2014_08
ORD IDord-937ea7c93b8e4d7c98344f9c5fbec190
Source noteuspto-grants-2014_08