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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227863Generated: October 30, 2026

Triethylamine → HCID 69733477, compound

https://huagongshe.com/reaction/2227863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantMethyl 4-aminomethylsalicylate hydrochlorideHCID 22556073—
SolventMethanolHCID 887—
ProductHCID 69733477HCID 6973347797.4%

Reaction Steps

Methyl 4-aminomethyl-2-hydroxybenzoate hydrochloride (10.9 g, 50 mmoles) was suspended in anhydrous methanol (200 mL) and di-tert-butyldicarbonate (10.9 g, 50 mmoles) and triethylamine (7.0 mL, 50 mmoles) were added. The solid rapidly dissolved with the slow evolution of gas. The reaction mixture was stirred at room temperature for 18 hours under dry nitrogen, then evaporated to dryness to afford a white amorphous mass. This mass was partitioned between ethyl acetate (200 mL) and water (100 mL). The layers were separated, and the ethyl acetate solution was dried over anhydrous sodium sulfate. The solution was filtered and evaporated to a white solid. This solid was crystallized from ethyl acetate/hexanes, filtered, and dried in vacuo to afford 13.7 g (97% yield) of methyl N-tert-butoxycarbonylaminomethyl-2-hydroxybenzoate (m.p. 95-96° C., open capillary, uncorrected).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414122B1
Source datasetuspto-grants-2002_07
ORD IDord-455dc541eeb24f69a93f96c045d1fd39
Source noteuspto-grants-2002_07