HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252449Generated: October 30, 2026
3,3-Dimethylbutylamine → HCID 57475711, compound
https://huagongshe.com/reaction/252449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3-Dimethylbutylamine | HCID 19709 | — |
| Reactant | 1-Methyl-2-imidazolecarboxaldehyde | HCID 139575 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57475711 | HCID 57475711 | — |
Reaction Steps
To a stirred solution of 3,3-dimethylbutyamine (2.81 g, 27.8 mmol) and 1-methyl-1H-imidazole-2-carbaldehyde (3.21 g, 29.1 mmol) in methanol (30 mL) at room temperature, sodium borohydride (1.05 g, 27.8 mmol) was added. The reaction mixture was then stirred at room temperature for 1 hour. The reaction mixture was concentrated, and hydrochloric acid (6 N, 5 mL) was then added. The resulting solution was washed with diethyl ether once. The aqueous phase was made basic by adding sodium hydroxide solution (3 N). The resulting solution was extracted with chloroform three times. The combined chloroform extracts were washed with brine and dried over magnesium sulfate. The solution was filtered and concentrated to yield (3,3-dimethyl-butyl)-(1-methyl-1H-imidazol-2-ylmethyl)-amine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868022B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-e44aa099c8b84d41a59c486050e2c556 |
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| Source note | uspto-grants-2011_01 |
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