HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218243Generated: October 29, 2026
Hydrochloric Acid → HCID 10125073, compound
https://huagongshe.com/reaction/218243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Ethylphenol | HCID 6997 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10125073 | HCID 10125073 | 95.7% |
Reaction Steps
Prepared according to Zaidlewicz, M.; et al; Tetrahedron:Asymmetry; 2003, 14, 1659-1664: Magnesium chloride (11.4 g, 120 mmol) was added at room temperature to a solution of 2-ethylphenol (9.77 g, 80 mmol) in acetonitrile (100 mL), followed by triethylamine (42 mL, 300 mmol). Paraformaldehyde (16.2 g, 540 mmol) was then added portionwise to the stirred suspension and the mixture was heated at reflux for 3 hours. The mixture was cooled to room temperature then poured into a vigorously stirred mixture of 250 mL of 5% HCl and 150 mL of diethyl ether. The organic phase was separated, and the aqueous layer re-extracted with 100 mL of ether. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure to give 11.5 g of 9 as a yellow oil which was used without further purification:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198302B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-7021500de3824ce1a3148b03e3b463ae |
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| Source note | uspto-grants-2012_06 |
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