HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470951Generated: October 29, 2026
4-Hydroxybenzyl Alcohol → [4-(2,2-Diethoxy-ethoxy)-phenyl]-methanol
https://huagongshe.com/reaction/470951
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [4-(2,2-Diethoxy-ethoxy)-phenyl]-methanol | HCID 57989210 | — |
Reaction Steps
Caesium carbonate (39.4 g) was added to a solution of 4-hydroxymethyl-phenol (10 g) and 2-bromo-1,1-diethoxyethane (12.73 mL) in DMF (200 mL) and the resulting mixture stirred at 90° C. for 16 h. The reaction was poured into water (500 mL) and extracted with ethyl acetate (3×250 mL). The combined organic solutions were washed with water (250 mL) and brine (250 mL), then dried over sodium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with an isohexane to diethyl ether gradient to give the subtitled compound as a yellow oil. Yield 9.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629271B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-95e384746b78438783d4c655c17300d0 |
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| Source note | uspto-grants-2014_01 |
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