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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85383Generated: October 25, 2026

Salicylic Acid → Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate

https://huagongshe.com/reaction/85383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylic AcidHCID 338—
ReactantImidazoleHCID 795—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBenzyl 3-aminobutan-2-ylcarbamateHCID 59193262—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamateHCID 6717490240%

Reaction Steps

To a mixture of benzyl 3-aminobutan-2-ylcarbamate (5.3 g, 23.8 mmol), 2-hydroxybenzoic acid (3.28 g, 23.8 mmol) and imidazole (1.62 g, 23.8 mmol) in EtOAc (180 mL) at 0° C. was slowly added a solution of DCC (4.90 g, 23.8 mmol) in EtOAc (20 mL). The reaction mixture was stirred (RT, 16 h), filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with PE-EtOAc (5:1) to afford benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate (3.2 g, 40%) as a colorless oil. Mass calculated for C19H22N2O4=342.39; found: [M+H]+=343.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846972B2
Source datasetuspto-grants-2014_09
ORD IDord-38642b5744a5467297104ac57dccd354
Source noteuspto-grants-2014_09