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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23786Generated: October 28, 2026

3-Hydroxybenzaldehyde → tert-Butyl (3-formylphenoxy)acetate

https://huagongshe.com/reaction/23786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
Reactanttert-ButanolHCID 6386—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Producttert-Butyl (3-formylphenoxy)acetateHCID 1497181636.5%

Reaction Steps

To a solution of 3-hydroxybenzaldehyde (5.00 g, 40.9 mmol) in DMF (40 mL) was added 1M potassium tert-butoxide in tert-butanol (40.9 mL, 40.9 mmol). The reaction was stirred for 2 minutes and tert-butyl bromoacetate (6.61 mL, 40.9 mmol) was added. The reaction was stirred for 1 hour and was quenched with 200 mL of water. The product was extracted into EtOAc and the organic solution was washed with water, dried over MgSO4, filtered and concentrated in vacuo. Purification via flash chromatography on silica gel (9:1 hexanes:EtOAc) afforded the title compound as a clear oil (3.53 g). 1H NMR (400 MHz, CDCl3) δ 9.94 (s, 1H), 7.48 (m, 2H), 7.32 (s, 1H), 7.21 (m, 1H), 4.56 (s, 2H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852863B2
Source datasetuspto-grants-2005_02
ORD IDord-f32d302f98954e75892077e067da114e
Source noteuspto-grants-2005_02