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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020798Generated: October 31, 2026

Dimethylformamide → HCID 66726685, compound

https://huagongshe.com/reaction/1020798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 66726488HCID 66726488—
ReactantHCID 66726651HCID 66726651—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66726685HCID 6672668552%

Reaction Conditions

Temperature60 °C

Reaction Steps

Intermediates 2-(4-bromo-3-(bromomethyl)-5-methylphenoxy)tetrahydro-2H-pyran and 2-(4-bromo-3,5-bis(bromomethyl)phenoxy)tetrahydro-2H-pyran from above reaction was made into a solution with 33 mL of DMF. The reaction mixture was then treated with KOAc (6.95 g, 70.83 mmol) before heating to 60° C. for 2 hr. The reaction was worked-up with equal volumes of water and CH2Cl2 (1:1, 50 mL). The layers were separated and the water phase was further extracted with equal volume of EtOAc before the organic layers were combined and dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure. The residue was purified by silica gel column using Combiflash to give 2-bromo-3-methyl-5-(tetrahydro-2H-pyran-2-yloxy)benzyl acetate (2.24 g, two steps 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716478B2
Source datasetuspto-grants-2014_05
ORD IDord-459e4b1ccb6944e4a0c7add014e1c54f
Source noteuspto-grants-2014_05