HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553404Generated: October 30, 2026
Hydrochloric Acid → 2-Methyl-4-(2-nitrobenzylamino)butanol
https://huagongshe.com/reaction/553404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Amino-2-methyl-1-butanol | HCID 10129911 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-4-(2-nitrobenzylamino)butanol | HCID 67461351 | 96.2% |
Reaction Steps
2-Nitrobenzaldehyde (7.33 g, 48.5 mmol) and 4-amino-2-methylbutanol (5.00 g, 48.5 mmol) were dissolved in toluene (50 ml) and heated to reflux for two hours with Dean Stark dehydration apparatus. After allowed to cool, the solvent was evaporated under reduced pressure. The obtained concentrate was dissolved in methanol (100 ml), added with sodium borohydride (2.75 g, 72.8 mmol) under ice cooled condition and stirred at the same temperature for two hours. The reaction mixture was further stirred at room temperature for two hours, adjusted to pH 4 by adding 1N hydrochloric acid, and the solvent was evaporated under reduced pressure. Water (30 ml) was added to dissolve the concentrate and after extracted with ethyl acetate, pH was adjusted to 8 by added a saturated sodium hydrogen carbonate aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to obtain 2-methyl-4-(2-nitrobenzylamino)butanol (11.12 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048825B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-9c5e9dd9f0e04c4ea754d9a84936acdd |
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| Source note | uspto-grants-2011_11 |
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