Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273652Generated: October 29, 2026

4-(6,7-Dimethyl-2-naphthyl)butanoic acid → 6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthrene

https://huagongshe.com/reaction/273652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(6,7-Dimethyl-2-naphthyl)butanoic acidHCID 22904592—
SolventMethanesulfonic AcidHCID 6395—
Product6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthreneHCID 22904595—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-(6,7-Dimethyl-2-naphthyl)butanoic acid (6.21 g, 0.026 mole) was added to 40 ml of CH3SO3H. The mixture was heated to 90° C. until all solid material disappeared (about 30 min.). The mixture was poured into ice and then extracted twice with ethylacetate. Combined ethylacetate solution was dried over anhydrous Na2SO4 and then concentrated. After flash chromatography on silica gel, 6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthrene was obtained as a pale yellow solid material (4.96 g, 0.022 mole, 85% yield). mp 114.0°-115.0° C., 1H NMR (CDCl3) δ2.12-2.20 (m,2H), 2.41 (s,3H), 2.47 (s,3H), 2.77 (t, J=6.4 Hz,2H), 3.09 (t, J=6.4 Hz,2H), 7.21 (d, J=8.3 Hz,1H), 7.54 (s,1H), 7.31 (d, J=8.3 Hz,1H), 9.20 (s,1 H), IR (KBr) cm-1 2930, 1669, 1590, 1510, Anal. Calcd. for C16H16O: C, 85.6: H, 7.19. Found: C, 86.00; H, 7.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387338
Source datasetuspto-grants-1995_02
ORD IDord-e0a6349ae7c9492f91d46604d665a059
Source noteuspto-grants-1995_02