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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845320Generated: October 30, 2026

Acetic Acid → HCID 54333419, compound

https://huagongshe.com/reaction/845320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAnilineHCID 6115—
ReactantHCID 21880474HCID 21880474—
SolventWaterHCID 962—
ProductHCID 54333419HCID 5433341958.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

Maleic anhydride is reacted with n-butylamine under the conditions reported by L. E. Coleman et al., in J. Org. Chem., 24: 135, (1959). A mixture containing the thus-formed n-butylmaleamic acid (12.0 g, 0.07 mol), anhydrous sodium acetate (2.7 g) and acetic anhydride (29 mL) is heated at 85° C. to 90° C. for 30 minutes. The solution is cooled to 40° C. and poured into 55 mL of water. The layers are stirred at room temperature for 15 minutes, the diluted to 275 mL. A dark oil precipitates. Extraction with 100 mL of CH2Cl2, then another 25 mL of CH2Cl2, and evaporation of solvent gives 9.9 g of n-butylmaleimide as an oil, ir, 1735 (sh) and 1700 cm-1. A solution of 9.9 g (0.065 mol) of the n-butylmaleimide and 35 mL of acetic acid is treated with 6.51 g (0.07 mol) of aniline, with the resulting solution heated at 120° C. for 30 minutes. The solution is cooled and poured into 280 mL of water. The amorphous material is collected and recrystallized from isopropyl alcohol to give 9.3 g of n-butyl anilinosuccinimide as off-white crystals, m.p. 97°-100° C., ir, 3350, 1720 (sh), 1680, 1600 cm-1; mass spec, (ci) m/e 247. Anal. Calcd. for C14H18N202: C, 68.29; H, 7.32; N, 11.38. Found: C, 68.46; H, 7.28; N, 11.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04757146
Source datasetuspto-grants-1988_07
ORD IDord-bc1c5f3008d2497e8859591cab11a1ab
Source noteuspto-grants-1988_07