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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280532Generated: November 1, 2026

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

https://huagongshe.com/reaction/2280532

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 numberUS09139516B2
Source datasetuspto-grants-2015_09
ORD IDord-c53a3f9766fe4e47996f76a97e0c3210
Source noteuspto-grants-2015_09