Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417365Generated: October 27, 2026

1,1'-Carbonyldiimidazole → Thalidomide

https://huagongshe.com/reaction/1417365

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. 1HNMR (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, CH2CH 2), 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 numberUS05877200
Source datasetuspto-grants-1999_03
ORD IDord-e4454a1370144876b18e66cd63c347ac
Source noteuspto-grants-1999_03