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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026860Generated: October 27, 2026

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

https://huagongshe.com/reaction/1026860

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 numberUS08729293B2
Source datasetuspto-grants-2014_05
ORD IDord-cdb1e4e8e30a4379adba96828f752476
Source noteuspto-grants-2014_05