HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354565Generated: October 28, 2026
Hydrochloric Acid → (E)-2,4-Dichloro-6-phenylmethoxycinnamaldehyde
https://huagongshe.com/reaction/354565
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 12 N 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 | US04375475 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-59a17bf264f545af9b54af5e1b0f4023 |
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| Source note | uspto-grants-1983_03 |
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