Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908121Generated: October 28, 2026

Benzene, [[(2-bromo-2-propenyl)oxy]methyl]- → HCID 58550929, compound

https://huagongshe.com/reaction/1908121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, [[(2-bromo-2-propenyl)oxy]methyl]-HCID 10857167—
ReactantHCID 58551005HCID 58551005—
CatalystPalladiumHCID 23938—
CatalystHCID 178454888HCID 178454888—
SolventDimethylformamideHCID 6228—
ProductHCID 58550929HCID 58550929—

Reaction Conditions

Temperature90 °C

Reaction Steps

Dichloro-[dicyclohexyl(phenyl)phosphaniumyl]-tritert-butylphosphaniumyl-palladium (981 mg, 0.150 mmol) and 2-bromoallyloxymethylbenzene (341 mg, 1.50 mmol) were dissolved in DMF (1 mL). A solution of benzyl 3-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (1.11 g, 3.00 mmol) in DMF (3 mL) was added the mixture was heated at 90° C. for 3 h. The mixture was then filtered through Celite using ethyl acetate. The filtrate was then washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue from step 1 was taken up in isopropanol (2 mL) and was added to 10% Pd/C (160 mg, 0.150 mmol). The vessel was purged with nitrogen and a balloon of hydrogen was added and the reaction mixture was allowed to stir overnight. The reaction mixture was filtered through Celite and the filtrate was concentrated. The residue was partitioned between aqueous 2M Na2CO3 and ethyl acetate. The layers were separated and the organic phase was discarded. To the aqueous phase was added 1M HCl until the solution was pH 3. The solution was then extracted with EtOAc (3×) and the combined organic layers were dried over sodium sulfate, filtered, and concentrated to provide 4-(1-hydroxypropan-2-yl)-3-methoxybenzoic acid. ESI-MS m/z calc 210.1. found 211.1 (M+1)+. Retention time: 1.19 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-182670de066043bbb8663a90ce6f79b6
Source noteuspto-grants-2013_12