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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Amino-2-methyl-1-butanolHCID 10129911—
SolventTolueneHCID 1140—
Product2-Methyl-4-(2-nitrobenzylamino)butanolHCID 6746135196.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048825B2
Source datasetuspto-grants-2011_11
ORD IDord-9c5e9dd9f0e04c4ea754d9a84936acdd
Source noteuspto-grants-2011_11