HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964711Generated: October 26, 2026
4-Chloroaniline → (4-Chloro-phenyl)-(neopentyl)-amine
https://huagongshe.com/reaction/964711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Chloro-phenyl)-(neopentyl)-amine | HCID 11424155 | 101.2% |
Reaction Steps
Pivalaldehyde (20.4 g, 236 mmol, 25.6 mL) was added to a solution of 4-chloroaniline (30.2 g, 236 mmol) in concentrated acetic acid (475 mL) at ambient temperature. After 1.5 hour, the reaction mixture was cooled to 0° C. and sodium borohydride (11.7 g, 307 mmol) was added portionwise over 15 minutes After stirring for 1 hour, the resulting mixture was diluted with water and extracted with ethyl acetate (3×). The combined organics were washed successively with water (3×), aqueous 2N sodium hydroxide (2×), saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give 47.2 g (99%) of the title compound as an off-white solid which was taken on crude to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05770594 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-911dcf046cd246e3ae6c1bf95a017eba |
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| Source note | uspto-grants-1998_06 |
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