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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantPivalaldehydeHCID 12417—
ReactantSodium borohydrideHCID 4311764—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product(4-Chloro-phenyl)-(neopentyl)-amineHCID 11424155101.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770594
Source datasetuspto-grants-1998_06
ORD IDord-911dcf046cd246e3ae6c1bf95a017eba
Source noteuspto-grants-1998_06