HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903079Generated: October 31, 2026
Hydrochloric Acid → 4-(Chloromethyl)-1-methoxy-2-(propan-2-yl)benzene
https://huagongshe.com/reaction/1903079
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Isopropylanisole | HCID 270623 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | 4-(Chloromethyl)-1-methoxy-2-(propan-2-yl)benzene | HCID 20467873 | — |
Reaction Steps
Hydrochloric acid gas is bubbed into a mixture of 55 g of o-isopropylanisole, 35 g of formaline and 9 g of zinc chloride with ice cooling and stirring for hours. The reaction mixture is added to ice water and the mixture is extracted with ether to give 70 g of crude 3-isopropyl-4-methoxybenzyl chloride. Potassium cyanide (26 g) is added to 400 ml of acetonitrile, 100 mg of 18-crown 6 is added thereto, and the benzyl chloride compound obtained above is dropped thereinto with refluxing and stirring. After the dropping is completed, the mixture is heated to reflux for ten hours with stirring. The reaction solution is then concentrated in vacuo, water is added to the concentrate, and the mixture is extracted with ether. The resulting extract is purified by subjecting to a distillation in vacuo to give 40 g of 3-isopropyl-4-methoxybenzyl cyanide, boiling point under 1 mm Hg 120°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04435397 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-5ad7e0ccd35449708d3bbe8fbce826b6 |
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| Source note | uspto-grants-1984_03 |
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