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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621249Generated: October 30, 2026

Trimethylamine → Methyl 3-cyano-4-hydroxybenzoate

https://huagongshe.com/reaction/1621249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
Reactant1,4-DioxaneHCID 31275—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantMethyl 4-hydroxy-3-iodobenzoateHCID 11346465—
SolventWaterHCID 962—
ProductMethyl 3-cyano-4-hydroxybenzoateHCID 11769089154.5%

Reaction Steps

(Boc)2O (44.7 g, 0.21 mol) was added portion-wise over 10 min to a 0° C. solution of compound 2 (42 g, 0.19 mol), trimethyl amine (51.9 mL, 0.37 mol), dioxane (140 L) and water (56 mL). After another 10 min, the ice bath was removed and the reaction mixture was stirred while warming to room temperature for another 2 hours. The reaction mixture was diluted in ethyl acetate (150 mL) and washed with 0.5 N HCl (200 mL×3). The organic layer was dried over magnesium sulfate, filtered, and the filtrate was concentrated in vacuo giving compound 3 (52 g, yield 97%) which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772507B2
Source datasetuspto-grants-2014_07
ORD IDord-2f00eb94fd9d4a719d02e7ad9759406f
Source noteuspto-grants-2014_07