Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845319Generated: October 31, 2026

Acetic Anhydride → HCID 21880474, compound

https://huagongshe.com/reaction/845319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantMaleic AnhydrideHCID 7923—
ReactantButylamineHCID 8007—
ReactantSodium AcetateHCID 517045—
ReactantHCID 20497288HCID 20497288—
SolventWaterHCID 962—
ProductHCID 21880474HCID 2188047492.3%

Reaction Conditions

Temperature40 °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-fc5b21bd22bf49b39ac04ab4d6d1232f
Source noteuspto-grants-1988_07