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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968481Generated: October 29, 2026

Sodium Hydroxide → 4-[(tert-Butoxycarbonyl)amino]-1-methyl-1H-imidazole-2-carboxylic acid

https://huagongshe.com/reaction/1968481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMETHYL 4-(TERT-BUTOXYCARBONYLAMINO)-1-METHYL-1H-IMIDAZOLE-2-CARBOXYLATEHCID 11379828—
SolventWaterHCID 962—
SolventOxolane--water (1/1)HCID 21881883—
Product4-[(tert-Butoxycarbonyl)amino]-1-methyl-1H-imidazole-2-carboxylic acidHCID 275722681.5%

Reaction Steps

Methyl 4-(tert-butoxycarbonylamino)-1-methyl-1H-imidazole-2-carboxylate (5.0 g, 19.59 mmol) in 120 ml of 1:1 THF/H2O was added 8 g of NaOH in 30 ml of water. The mixture was stirred overnight, concentrated, diluted with water, extracted with EtAc/Hexane (1:1). The aqueous solution was adjusted to pH 4.0 with 20% H3PO4 and extracted with EtAc (4×60 ml). The organic solutions were combined, dried over MgSO4, filtered, evaporated and crystallized with ethanol/EtAc/Hexane to afford 3.85 g (81%) of the title product. 1H NMR (DMSO) 9.32 (s, 1H), 7.29 (s, 1H), 3.57 (s, 3H), 1.42 (s, 9H); 13C NMR 172.45, 159.78, 136.93, 135.44, 132.85, 79.50, 35.57, 28.07; MS m/z− 240.8 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426402B2
Source datasetuspto-grants-2013_04
ORD IDord-0c4554504eb5469fb28105de1eb5ae6a
Source noteuspto-grants-2013_04