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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322532Generated: October 30, 2026

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

https://huagongshe.com/reaction/322532

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 15-1 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 15-2 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211184B1
Source datasetuspto-grants-2001_04
ORD IDord-6b3d4a734dca402ebd3bc334e8db2ec9
Source noteuspto-grants-2001_04