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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267295Generated: November 1, 2026

Hydrochloric Acid → (E)-3-(4-{[2-(1H-indol-3-yl)-ethylamino]-methyl}-phenyl)-acrylic acid methyl ester

https://huagongshe.com/reaction/1267295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTryptamineHCID 1150—
Reactant2-Propenoic acid, 3-(4-formylphenyl)-HCID 98077—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 3-(4-formylphenyl)-2-propenoateHCID 53401287—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
SolventPotassium CarbonateHCID 11430—
Product(E)-3-(4-{[2-(1H-indol-3-yl)-ethylamino]-methyl}-phenyl)-acrylic acid methyl esterHCID 1089299986.7%

Reaction Steps

4-formylcinnamic acid methylester is produced by adding 4-formylcinnamic acid (25 g, 0.143 mol) in MeOH and HCl (6.7 g, 0.18 mol). The resulting suspension is heated to reflux for 3 hours, cooled and evaporated to dryness. The resulting yellow solid is dissolved in EtOAc, the solution washed with saturated NaHCO3, dried (MgSO4) and evaporated to give a pale yellow solid which is used without further purification (25.0 g, 92%). To a solution of tryptamine (16.3 g, 100 mmol) and 4-formylcinnamic acid methylester (19 g, 100 mmol) in dichloroethane, NaBH(OAc)3 (21 g, 100 mmol) is added. After 4 hours the mixture is diluted with 10% K2CO3 solution, the organic phase separated and the aqueous solution extracted with CH2Cl2. The combined organic extracts are dried (Na2SO4), evaporated and the residue purified by flash chromatography to produce 3-(4-{[2-(1H-indol-3-yl)-ethylamino]-methyl}-phenyl)-(2E)-2-propenoic acid methyl ester (29 g). A solution of KOH (12.9 g 87%, 0.2 mol) in MeOH (100 mL) is added to a solution of HONH2.HCl (13.9 g, 0.2 mol) in MeOH (200 mL) and a precipitate results. After 15 minutes the mixture is filtered, the filter cake washed with MeOH and the filtrate evaporated under vacuum to approximately 75 mL. The mixture is filtered and the volume adjusted to 100 mL with MeOH. The resulting solution 2M HONH2 is stored under N2 at −20° C. for up to 2 weeks. Then 3-(4-{[2-(1H-indol-3-yl-ethylamino]-methyl}-phenyl)-(2E)-2-propenoic acid methyl ester (2.20 g, 6.50 mmol) is added to 2 M HONH2 in MeOH (30 mL, 60 mmol) followed by a solution of KOH (420 mg, 6.5 mmol) in MeOH (5 mL). After 2 hours dry ice is added to the reaction and the mixture is evaporated to dryness. The residue is dissolved in hot MeOH (20 mL), cooled and stored at −20° C. overnight. The resulting suspension is filtered, the solids washed with ice cold MeOH and dried under vacuum, producing N-Hydroxy-3-[4-[[[2-(1H-indol-3-yl)-ethyl]-amino]methyl]phenyl]-2E-2-propenamide (m/z 336 [MH+]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552065B2
Source datasetuspto-grants-2003_04
ORD IDord-4ab1ace6286f416981168cb478a03f59
Source noteuspto-grants-2003_04