HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427462Generated: November 2, 2026
Hydrochloric Acid → 2,6-Dichloro-4-hydroxybenzaldehyde
https://huagongshe.com/reaction/2427462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tert-butyl(3,5-dichlorophenoxy)dimethylsilane | HCID 18007485 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Dichloro-4-hydroxybenzaldehyde | HCID 528382 | — |
Reaction Steps
Dissolve tert-butyl-(3,5-dichloro-phenoxy)-dimethyl-silane (425 g, 1.5 mol) in 4 L dry tetrahydrofuran and cool to −68° C. Slowly add 1.1 equivalents of sec-butyl lithium (103.1 g, 1.61 mol) at −68° C. (˜1.75 hr). After addition is complete, stir the reaction at −70° C. for 30 min. Add dimethylformamide (168.5 g, 2.3 mol) and stir the reaction at −70° C. for 1 hr. Add 1 M hydrochloric acid in water (3.5 L) and allow the reaction to warm to room temperature. Pour the reaction mixture into ether (5 L), wash with water then brine. Dry over sodium sulfate and concentrate under vacuum to an orange solid. Triturate with cold dichloromethane and filter to recover 250 g (80%) pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968585B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-b6d227f573024d048c5b2a323a5eef4d |
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| Source note | uspto-grants-2011_06 |
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