Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375012Generated: October 27, 2026

Water → 6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthrene

https://huagongshe.com/reaction/375012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant11-Iodoundec-1-eneHCID 11119462—
Reactant6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthreneHCID 22904595—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
Product6,7-Dimethyl-4-oxo-3-(10-undecenyl)-1,2,3,4-tetrahydrophenanthreneHCID 2290458839%
Product6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthreneHCID 2290459547%

Reaction Conditions

Temperature60 °C

Reaction Steps

t-BuOK (3.6 g, 0.032 mole) was dissolved in 250 ml of dry benzene at 40°-50° C. To the stirred solution was added 6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthrene (3.6 g, 0.016 mole) in 50 ml of dry benzene and then, 10-undecenyl iodide (4.58 g, 0.016 mole) at 30° C. under N2. The mixture was heated to 60° C. for 2.5 hr under N2. After cooling the reaction mixture to room temperature, water was added. The whole mixture was extracted twice with diethylether. The combined diethylether solution was dried over anhydrous MgSO4 and then concentrated. Flash column chromatography of the residue on silica gel afforded 6,7-Dimethyl-4-oxo-3-(10-undecenyl)-1,2,3,4-tetrahydrophenanthrene as a sticky brown solid (2.36 g, 0.0063 mole, 39% yield) as a desired product, and unreacted 6,7-Dimethyl-4-oxo-1,2,3,4-tetrahydrophenanthrene (1.70 g, 47% recovered). 1H NMR (CDCl3)δ 1.29-1.62 (m,14H), 1.86-2.08 (m,4H), 2.21-2.35 (m,2H), 2.40 (s,3H), 2.46 (s,3H), 2.52-2.63 (m,1H), 3.07-3.13 (m,2H), 4.90-5.04 (m,2H), 5.75-5.89 (m,1H), 7.17 (d, J=8.2 Hz,1H), 7.53 (s,1H), 7.77 (d, J=8.2 Hz,1H), 9.10 (s,1H), IR (KBr) cm-1 2920, 2850, 1669, 1600, exact (EI) mass. calcd. for C27H36O: 376.2766, Found: 376.2766.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484530
Source datasetuspto-grants-1996_01
ORD IDord-a0db89e094b44644acf1d5e3c1adcb53
Source noteuspto-grants-1996_01