HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892257Generated: October 30, 2026
Hydrochloric Acid → HCID 22242089, compound
https://huagongshe.com/reaction/892257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde | HCID 22242092 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22242089 | HCID 22242089 | 81.6% |
Reaction Steps
8.50 g (224 mmol) lithium aluminium hydride were given to 250 ml Tetrahydrofuran (THF) and stirred for 20 min. A solution of 19.4 g (110 mmol) 4-allyloxy-2-methyl-benzaldehyde in 100 ml THF was added dropwise and stirring continued for 3 h. The reaction mixture was cooled to 0° C., carefully hydrolysed with 40 ml concentrated ammonium chloride solution, stirred for 60 min. and adjusted to pH=5 with conc. hydrochloric acid. A formed salt precipitate was removed by filtration, washed with THF and the combined organic solutions evaporated. Chromatography of the residue on silica (n-heptane/ethyl acetate 1:3) gave 16.0 g (81%) (4-allyloxy-2-methyl-phenyl)-methanol as a slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005526B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-3d23fc54cb0143c88a45eb776c75b6fd |
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| Source note | uspto-grants-2006_02 |
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