HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494886Generated: October 30, 2026
4-Bromothiophenol → 1-Bromo-4-[(2,2-diethoxyethyl)sulfanyl]benzene
https://huagongshe.com/reaction/494886
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromothiophenol | HCID 66049 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Bromo-4-[(2,2-diethoxyethyl)sulfanyl]benzene | HCID 11833671 | 96.5% |
Reaction Steps
1-Bromo-4-[(2,2-diethoxyethyl)thio]benzene (Chemical Abstracts number 96804-05-6) was prepared as described in Banfield et al.; J. Chem. Soc.; 1956; 2603-2607, and in Amin, et al.; J. Chem. Soc. Perkin Trans. 2; 1982; 1489-1492. 4-Bromothiophenol (20 g, 95%) in ethanol (80 mL) was treated with 21 wt % of sodium ethoxide in ethanol (36 g, 1.05 eq). The solution was heated at 55° C. for 30 minutes and bromoacetaldehyde diethylacetal (22.56 g, 1.05 eq) was added. The mixture was heated at reflux for 10 hours, ethanol was removed and the residue was diluted with 80 mL of water. The product was extracted with 2×120 mL of ethyl acetate. The combined ethyl acetate layer was washed with 2×40 mL of 15% NaCl and concentrated under vacuum to a brown oil (32.0 g, 92.5% potency, 96.5% yield). The product can be further purified by column chromatography (silica gel, 5:95 EtOAc:hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538138B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a1e949ab39e14f5097e23a136b009c51 |
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| Source note | uspto-grants-2009_05 |
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