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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451837Generated: October 27, 2026

1,1'-Carbonyldiimidazole → Thalidomide

https://huagongshe.com/reaction/1451837

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) δ 11.16 (s, 1 H, NH), 8.05-7.80 (br s, 4 H, Ar), 5.18 (dd, 1 H, J=12, 5 Hz, CHCO), 3.05-2.85 (m, 1 H, CH2CO), 2.70-2.45 (m, 2 H, CH2CH2), 2.15-2.00 (M, 1 H, CH2). 13C NMR (DMSO-d6) δ 172.8, 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 numberUS05605914
Source datasetuspto-grants-1997_02
ORD IDord-eb95e671ded44d70b0cf5a9bc77f928b
Source noteuspto-grants-1997_02