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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027756Generated: October 29, 2026

Imidazole → tert-butyl 2-(2-hydroxy-N-methylbenzamido)ethylcarbamate

https://huagongshe.com/reaction/1027756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantSalicyloyl chlorideHCID 74041—
ReactantN-(tert-Butoxycarbonyl)-N'-methylethylenediamineHCID 3435744—
SolventEthyl AcetateHCID 8857—
Producttert-butyl 2-(2-hydroxy-N-methylbenzamido)ethylcarbamateHCID 5919331934%

Reaction Steps

To a mixture of tert-butyl 2-(methylamino)ethylcarbamate (0.348 g, 2 mmol), 2-hydroxybenzoyl chloride (0.276 g, 2 mmol) and imidazole (0.136 g, 2 mmol) in ethyl acetate (8 mL) at 0° C. was slowly added a solution of DCC (0.412 g, 2 mmol) in ethyl acetate (2 mL). The mixture was stirred (RT, 16 h), filtered and concentrated under reduced pressure. The crude material was purified by chromatography on silica gel, eluting with ethyl acetate/petroleum ether (20-50%) to afford tert-butyl 2-(2-hydroxy-N-methylbenzamido)ethylcarbamate (0.2 g, 34%) as a colorless oil. 1HNMR (CDCl3): δ7.5 (m, 2H, CH), 7.0 (d, 1H, CH), 6.8 (d, 1H, CH), 3.7 (m, 2H, CH2), 3.48 (m, 2H, CH2), 3.2 (m, 3H, CH3), 1.5 (s, 9H, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735378B2
Source datasetuspto-grants-2014_05
ORD IDord-3fab298fff2146de8f96ad79dfb305e5
Source noteuspto-grants-2014_05