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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417372Generated: November 1, 2026

Ammonium Hydroxide → 2-Phthalimido-4-methylpentanamide

https://huagongshe.com/reaction/1417372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methylpentanoic acidHCID 102808—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Phthalimido-4-methylpentanamideHCID 278725489.1%

Reaction Steps

To a stirred solution of 2-phthalimido-4-methylpentanoic acid (1.32 g, 5.0 mmol) in tetrahydrofuran (25 mL) are added carbonyldiimidazole (0.81 g, 5.0 mmol) and a few crystals of 4-N,N-dimethylaminopyridine followed by 15 mL of tetrahydrofuran. The reaction mixture is stirred at room temperature for 1 hour, then 1 mL of concentrated ammonium hydroxide is added. After 10 minutes, the reaction mixture is diluted with 50 mL water. The resulting slurry is partially concentrated to remove the tetrahydrofuran and filtered. The solid is washed with water and dried in vacuo (60° C., <1 mm) to afford 1.16 g (89%) of 2-phthalimido-4-methylpentanamide as a white powder: mp 173°-176° C.; 1H NMR (DMSO-d6, 250 MHz) δ 7.95-7.79 (m, 4 H, Ar), 7.61 (br s, 1 H, CONH2), 7.22 (br s, 1 H, CONH2), 4.73-4.60 (m, 1 H), 2.30-2.10 (m, 1 H), 1.95-1.80 (m, 1H), 1.45-1.25 (m, 1H); 13C NMR (DMSO-d6) d: 170.4, 167.7, 134.4, 131.5, 123.1, 51.3, 36.4, 24.7, 23.2, 20.6. Anal. Calculated for C14H16N2O3. Theoretical: C, 64.60; H, 6.20; N, 10.76. Found: C, 64.63; H, 6.11; N, 10.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877200
Source datasetuspto-grants-1999_03
ORD IDord-77ed9d7ddb564a869dbcca18f49ee6fe
Source noteuspto-grants-1999_03