HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372833Generated: October 30, 2026
Hydrochloric Acid → HCID 20326853, compound
https://huagongshe.com/reaction/372833
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(Aminomethyl)-4-tert-butyl-6-(trifluoromethyl)phenol | HCID 12652145 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20326853 | HCID 20326853 | — |
Reaction Steps
The solid, the 2-chloroacetyl derivative of 2-aminomethyl-4-(1,1-dimethylethyl)-6-trifluoromethylphenol is dissolved in a mixture of ethanol (75 ml.) and 12 N hydrochloric acid (25 ml.). The mixture is refluxed for 5 hours, cooled to 20° C. and diluted with 12 N hydrochloric acid (150 ml.). Upon cooling to -20° C., the product separates (14 g.). It is crystallized from ethanol-12 N hydrochloric acid (1:4) to obtain pure 2-aminomethyl-4-tertbutyl-6-trifluoromethylphenol hydrochloride, m.p. 202°-204° C. This material is added to 500 ml. of warm water and treated with excess ammonium hydroxide. The precipitate is collected, washed with water, and air dried to give the free base, m.p. about 148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04092414 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-df1ce4fbca984e95a2ed6531e6f7f0ff |
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| Source note | uspto-grants-1978_05 |
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