HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987848Generated: October 30, 2026
Ammonium Chloride → 3-Acetoxymethyl-2,4,6-trimethylaniline
https://huagongshe.com/reaction/987848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Acetoxymethyl-3-nitro-2,4,6-trimethylbenzene | HCID 15254286 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Acetoxymethyl-2,4,6-trimethylaniline | HCID 10655942 | 75% |
Reaction Steps
To a solution of 1-acetoxymethyl-3-nitro-2,4,6-trimethybenzene (6.0 g, 25.2 mmol) in methanol (100 mL) were sequentially added ammonium chloride (2.7 g in 25 mL of water), zinc powder (11 g). The exothermic reaction was vigorously stirred until it was back to RT (2 h). To work up the crude mixture was filtered off and the cake was washed with methanol. The methanolic solutions were concentrated to a volume of 20 mL, added 1 N HCl (300 mL). The insoluble material was removed by filtration, the solution was basified with solid NaHCO3. The semicrystalline precipitate was taken into ethyl acetate. The extract was concentrated and the residual product purified by means of column chromatography (25% ethyl acetate/hexane) to give 3-Acetoxymethyl-2,4,6-trimethylaniline as a pink oil (3.8 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06632829B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-2f37468629814e559787194c6e201e63 |
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| Source note | uspto-grants-2003_10 |
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