HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702602Generated: October 26, 2026
Hydrochloric Acid → alpha-Allenyl-3-phenoxybenzyl alcohol
https://huagongshe.com/reaction/1702602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 3-Phenoxy-alpha-ethynylbenzylalcohol | HCID 12919092 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | alpha-Allenyl-3-phenoxybenzyl alcohol | HCID 13104645 | — |
Reaction Steps
10 g of α-ethynyl-3-phenoxybenzyl alcohol, 2.1 g of paraformaldehyde, 5.3 g of diisopropylamine, 0.215 g of CuBr and 50 ml of dioxane are refluxed for 2 hours. The reaction mixture is cooled to 20° C., poured into a solution of 2 N HCl and extracted with ether. The organic phase is washed with 10% potassium carbonate and saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The residue is chromatographed over silica gel with a 7:3 mixture of hexane/ether as eluant, affording the compound of the formula ##STR5## with a refractive index of nD20° =1.5942.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04348408 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-bef36a2472e643a9af1854f541dd8bdf |
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| Source note | uspto-grants-1982_09 |
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