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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514306Generated: October 30, 2026

2,5-Dihydroxybenzoic acid → HCID 66746377, compound

https://huagongshe.com/reaction/514306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dihydroxybenzoic acidHCID 3469—
ReactantEthyl AcetateHCID 8857—
Reactant552302-36-0HCID 10262406—
ReactantHCID 11508769HCID 11508769—
SolventEthanolHCID 702—
ProductHCID 66746377HCID 6674637791%

Reaction Steps

(2S)-(4E)-N-Methyl-5-(5-methoxy-3-pyridinyl)-4-penten-2-amine 2,5-dihydroxybenzoate A hot solution of 2,5-dihydroxybenzoic acid (gentisic acid) (0.582 g, 3.78 mmol) in absolute ethanol (1 mL) was added to a warm solution of (2S)-(4E)-N-methyl-5-(5-methoxy-3-pyridinyl)-4-penten-2-amine (1.00 g, 4.85 mmol, 86.7% E isomer by GC-FID) in absolute ethanol (1 mL), using additional ethanol (2 mL) in the transfer. The resulting mixture was concentrated via rotary evaporation, leaving 1.5 mL of ethanol in the solution. With stirring and heating to near reflux, crystallization occurred. The resulting hot mixture was treated drop-wise with ethyl acetate (5.5 mL). After cooling to room temperature, the mixture was further cooled at 5° C. for 48 h. The resulting solids were filtered, washed with ethyl acetate (2×5 mL) and dried at 50° C. to give 1.24 g (91%) of an off-white powder (98.0% E isomer by GC-FID for the free base). To remove the color from the sample, the material was recrystallized from ethanol/isopropanol (3.5 mL: 5.5 mL) to give 1.03 g (83% recovery) of an off-white powder and subsequently recrystallized from ethanol/ethyl acetate (3 mL: 12 mL) to give 0.90 g (87% recovery) of a white, crystalline powder, mp 166-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107915B2
Source datasetuspto-grants-2015_08
ORD IDord-887f768784c54bca996171f57a95a154
Source noteuspto-grants-2015_08