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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464697Generated: October 29, 2026

Acetic Acid → 5-Methoxy-3-(N-methylthioethyl-N-propionylamino)chroman

https://huagongshe.com/reaction/1464697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantPropionyl chlorideHCID 62324—
Reactant(2-(Methylthio)ethyl)amineHCID 87697—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Methoxy-3-ChromanoneHCID 11769096—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Methoxy-3-(N-methylthioethyl-N-propionylamino)chromanHCID 1470343164%

Reaction Steps

To a solution of the appropriate amine (400 mg, 2.27 mmol) and acetic acid (400 mg, 6.99 mmol) in absolute ethanol (10 ml) was added 5-methoxy-3-chromanone (250 mg, 1.40 mmol), followed by 2-methylthioethylamine (0.6 ml, 6.41 mmol). The solution was stirred with 4 Å molecular sieve for 1 hour 15 min. MeOH (25 ml) was added to the reaction mixture and sodium cyano-borohydride (1.5 g, 23.6 mmol) dissolved in MeOH (10 ml). The reaction mixture was stirred for 30 min, water was added (50 ml) and pH adjusted with 5% aqueous NaOH to 11. The mixture was extracted with CH2Cl2. The phases were separated and the organic layer washed with water, dried (Na2SO4) and the solvent was evaporated. The crude product was immediately propionylated with propionyl chloride (0.5 ml, 5.72 mmol) in CH2Cl2 (20 ml) containing triethylamine (1 ml, 7.2 mmol). The reaction mixture was stirred for 30 min, washed with aqueous sodium carbonate solution, 1N HCl and water. The organic layer was separated and dried (MgSO4). The solvent was evaporated and the crude product chromatographed (SiO2) with light petroleum-ether (1:1) as eluant yielding 276 mg (64%) of the product as an oil. GC/MS (HP-5970A), m/e=310 (0.2) M+, 162 (100), 161 (54), 163 (50), 192 (22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306830
Source datasetuspto-grants-1994_04
ORD IDord-59f3d643ac3e4c6396db09774f68a709
Source noteuspto-grants-1994_04