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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555587Generated: October 30, 2026

2,5-Dihydroxybenzoic acid → HCID 11508769, compound

https://huagongshe.com/reaction/555587

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dihydroxybenzoic acidHCID 3469—
ReactantEthyl AcetateHCID 8857—
Reactant552302-36-0HCID 10262406—
SolventEthanolHCID 702—
ProductHCID 11508769HCID 1150876991%

Reaction Steps

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 numberUS08053451B2
Source datasetuspto-grants-2011_11
ORD IDord-9b3037341607458d87479329da324422
Source noteuspto-grants-2011_11