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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730371Generated: October 29, 2026

Trimethylamine → Methyl 3-cyano-4-hydroxybenzoate

https://huagongshe.com/reaction/730371

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, 0.21mol) 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 mL) 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 numberUS07582668B2
Source datasetuspto-grants-2009_09
ORD IDord-6f090e7326ba41b8913d7a9ec8a964a9
Source noteuspto-grants-2009_09