Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940053Generated: November 1, 2026

1,1'-Carbonyldiimidazole → Thalidomide

https://huagongshe.com/reaction/1940053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-Phthaloyl-L-glutamineHCID 259136—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductThalidomideHCID 542690%

Reaction Steps

A stirred mixture of N-phthaloyl-L-glutamine (48.0 g, 174 mmoL), carbonyldiimidazole (30.43 g, 188 mmoL), and 4-dimethylaminopyridine (0.105 g, 0.861 mmoL) in anhydrous tetrahydrofuran (300 mL) is heated to reflux for 16 hours. The reaction slurry is filtered and the solid washed with methylene chloride (200 mL). The solid is air-dried and then dried in vacuo (60° C., <1 mm) to afford 40.40 g (90%) of thalidomide as a white powder. 1H NMR (DMSO-d6) δ11.16 (s, 1H, NH), 8.05-7.80 (br s, 4H, Ar), 5.18 (dd, 1H, J=12, 5 Hz, CHCO), 3.05-2.85 (m, 1H, CH2CO), 2,70-2.45 (m, 2H, CH2CH2) 2.15-2.00 (M, 1H, CH2). 13C NMR (DMSO-d6) δ172.8, 169.8, 167.1, 134.9, 131.2, 123.4, 49.0, 30.9, 22.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698579
Source datasetuspto-grants-1997_12
ORD IDord-a197121e6131442d908ed6a59cfdd88e
Source noteuspto-grants-1997_12