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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421288Generated: November 4, 2026

Ammonium Hydroxide → HCID 21250949, compound

https://huagongshe.com/reaction/1421288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantN-PhthaloylglycineHCID 20825—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21250949HCID 2125094976%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of N-phthaloylglycine (2.50 g, 8.89 mmol) in tetrahydrofuran (50 mL) is add ed carbonyldiimidazole (1.50 g, 9.25 mmol) and a few crystals of 4-NN-dimethylaminopyridine. The reaction is then heated to 50° C. for 45 minutes. After the reaction mixture had cooled to room temperature, 1 mL of concentrated ammonium hydroxide is added via syringe. The reaction is stirred for 1 hour, then diluted with 50 mL of water and partially concentrated to remove the majority of the tetrahydrofuran. The resulting slurry was filtered and the solid washed with copious amounts of water. The solid was dried in vacuo (60° C.,<1 mm) to afford 1.9 g (76%) of α-phthalimidophenyl-acetamide as an off-white powder: mp 218-220.C; H NMR (DMSO-d6)δ 9.00-7.75 (m, 4H, Ar), 7.61 (br s, 1H, CONH2), 7.55-7.20 (m, 6H, Ar, CONH2), 5.82 (s, 1H, CHCO2); 13C NMR (DMSO-d6)δ 168.2, 167.1, 135.6, 134.5, 131.4, 129.4, 127.9, 127.7, 123.1, 56.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06075041
Source datasetuspto-grants-2000_06
ORD IDord-8d63ca06d86645a1835e3ded40e9ba8c
Source noteuspto-grants-2000_06