HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218245Generated: October 30, 2026
Hydrochloric Acid → HCID 18963024, compound
https://huagongshe.com/reaction/218245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Ethylbenzene-1,2-diol | HCID 70278 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18963024 | HCID 18963024 | 75.2% |
Reaction Steps
Magnesium chloride (1.71 g, 18 mmol) was added at room temperature to a solution of 10 (1 g, 7.2 mmol) in acetonitrile (10 mL), followed by triethylamine (6.3 mL, 45 mmol). Paraformaldehyde (1.47 g, 49 mmol) was then added portionwise to the stirred suspension and the mixture was heated at reflux for 2 hours. The mixture was cooled to room temperature then poured into a vigorously stirred mixture of 50 mL of 5% HCl and 50 mL of diethyl ether. The organic phase was separated, and the aqueous layer re-extracted with 50 mL of ether. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure to give a crude which was purified by column (cyclohexane:AcOEt 6:1) to give 0.9 g of 11:
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-5146c969ce2a40989e4964e0b17f31bb |
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| Source note | uspto-grants-2012_06 |
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