Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850587Generated: October 30, 2026

3-Bromophenol → 1-Bromo-3-(2,2-diethoxyethoxy)benzene

https://huagongshe.com/reaction/850587

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
ReactantSodium hydrideHCID 24758—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
SolventDimethylformamideHCID 6228—
Product1-Bromo-3-(2,2-diethoxyethoxy)benzeneHCID 15453765—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of NaH (2.77 g, 115.6 mmol) in DMF (100 mL) at 0° C. was added a solution of 3-bromophenol 1-1 in DMF (40 mL) over 40 min. After the addition was complete, the solution was stirred for an additional 30 min. The solution was then treated with neat bromoacetaldehyde diethyl acetal (17.36 g, 115.6 mmol). The solution was heated at 100° C. for 8 h, cooled to room temperature, and extracted with Et2O (3×200 mL). The combined organic extracts were washed with 10% aq. NaOH (100 mL) and brine (100 mL), dried over MgSO4, filtered and concentrated to give 1-2 as a yellow oil. TLC Rf=0.4 (10% ethyl acetate/hexanes). 1H NMR (300 MHz, CDCl3) δ 7.19-7.05 (m, 3H), 6.85 (d, 1H), 4.81 (t, 1H, J=6.8 Hz), 3.99 (d, 2H, J=6.8 Hz), 3.71 (m, 4H), 1.22 (t, 6H, J=7.1 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017926
Source datasetuspto-grants-2000_01
ORD IDord-84ac66542ddb43fd976dc036993eff44
Source noteuspto-grants-2000_01