HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824913Generated: October 28, 2026
3-Bromophenol → 1-Bromo-3-(2,2-diethoxyethoxy)benzene
https://huagongshe.com/reaction/1824913
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromophenol | HCID 11563 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-3-(2,2-diethoxyethoxy)benzene | HCID 15453765 | 101.7% |
Reaction Steps
A solution of 10 gm (57.8 mMol) 3-bromophenol in 25 mL dimethylformamide was added dropwise to a mixture of 2.8 gm (70 mMol) sodium hydride (60% suspension in mineral oil) in 30 mL dimethylformamide. The reaction mixture was stirred for one hour after the addition was complete. To the reaction mixture was then added 9.7 mL (64.5 mMol) bromoacetaldehyde diethyl acetal and the resulting mixture was stirred at 153° C. for 2 hours. The reaction mixture was then allowed to cool to room temperature and was diluted with 300 mL diethyl ether. This mixture was then washed with two 150 ml portions of water, washed with 50 mL saturated aqueous sodium chloride, dried over magesium sulfate and concentrated under reduced pressure to provide about 17 gm of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045545B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-a2ff8467d08d4465b2ff2fc3c6b532fd |
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| Source note | uspto-grants-2006_05 |
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