HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986050Generated: October 31, 2026
Hydrochloric Acid → (E)-2,4-Dichloro-6-phenylmethoxycinnamaldehyde
https://huagongshe.com/reaction/986050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,4-Dichloro-6-phenylmethoxybenzaldehyde | HCID 12802881 | — |
| Solvent | Acetaldehyde | HCID 177 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-2,4-Dichloro-6-phenylmethoxycinnamaldehyde | HCID 12802888 | 33% |
Reaction Steps
A stirred suspension of 2,4-dichloro-6-phenylmethoxybenzaldehyde (15.5 g, 55.1 mmole) in acetaldehyde (30 ml) was cooled to 5° C. and treated with 25% methanolic potassium hydroxide (1.4 ml, 6.24 mmole) at such a rate that the internal temperature was maintained at 25°-30° C. The resulting solution was stirred for 30 minutes in the ice bath, treated with acetic anhydride (30 ml) and then heated at 100° C. for 30 minutes. After cooling to 30° C. the solution was treated with water (84 ml) and 12N hydrochloric acid (7 ml). The resulting mixture was refluxed for 30 minutes and then cooled in an ice bath to give a gummy solid which was recrystallized from cyclohexane to give the title compound (5.6 g, 33%), mp 109°-112° C.: pmr (CDCl3)δ5.10 (2H, s), 7.33 (5H, s), 9.68 (H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04710513 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-90f6e014e1e847b39ba744af46d0621f |
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| Source note | uspto-grants-1987_12 |
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