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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773028Generated: November 2, 2026

Benzyl Bromide → HCID 86731481, compound

https://huagongshe.com/reaction/1773028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86731482HCID 86731482—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86731481HCID 8673148176.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a flask containing 1-methoxy-4-oxocyclohexanecarboxylic acid (0.253 g, 1.469 mmol) was added potassium carbonate (0.406 g, 2.94 mmol). The mixture was diluted with DMF (5 mL) and benzyl bromide (0.192 mL, 1.616 mmol) was added. The mixture was heated to 60° C. for 15.5 h, then cooled to rt, diluted with water (20 mL), and extracted with ethyl acetate (20 mL). The organic layer was washed with water three times, then with sat. aq. NaCl, and was finally dried over magnesium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography using a 0-50% EtOAc in hexanes gradient and a 12 g silica gel column to give the title product (0.294 g, 1.12 mmol, 76% yield). 1H NMR (500 MHz, CHLOROFORM-d) δ=7.41-7.31 (m, 5H), 5.23 (s, 2H), 3.35 (s, 3H), 2.62-2.53 (m, 2H), 2.37-2.28 (m, 4H), 2.19-2.10 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249180B2
Source datasetuspto-grants-2016_02
ORD IDord-49bae75efc0a40a181c17056c21ecbf5
Source noteuspto-grants-2016_02