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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368885Generated: October 30, 2026

3-Hydroxyacetophenone → HCID 22128939, compound

https://huagongshe.com/reaction/368885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventDimethylformamideHCID 6228—
ProductHCID 22128939HCID 2212893983%

Reaction Steps

To a suspension of NaH (60% dispersion in mineral oil, 1.47 g, 36.7 mmol) in anhydrous DMF (50 mL) at 0° C. was added solid 3'-hydroxyacetophenone (5.0 g, 36.7 mmol). The mixture was stirred under N2 for 10 min and a clear yellow solution was formed. Then, tert-butylbromoacetate (6.23 mL, 38.5 mmol) was added and the mixture stirred at 0° C. for 5 min and then at room temperature for 20 min. TLC showed no starting material remaining. The mixture was partitioned between EtOAc (250 mL) and water (100 mL). The organic layer was separated, washed with saturated brine, dried (MgSO4) and concentrated in vacuo. Chromatography on silica (20% EtOAc/hexanes) gave 7.6 g (83%) of a white crystal. 1H NMR (CDCl3, 300 MHz) 7.60-7.14 (m, 4 H), 4.59 (s, 2 H), 2.60 (s, 3 H), 1.51 (s, 9 H); 13C NMR (CDCl3, 75 MHz) 198.0, 168.0, 158.6, 138.9, 130.1, 122.3, 120.6, 113.5, 83.0, 66.1, 28.4, 27.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133456
Source datasetuspto-grants-2000_10
ORD IDord-a1f626395ef5449aa433099822b6bc43
Source noteuspto-grants-2000_10