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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366265Generated: October 30, 2026

Water → (2R)-N-methyl-2-methylamino-3-(thiophen-2-yl)propionamide

https://huagongshe.com/reaction/366265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantN-Methyl-N-((1R)-1-(methylcarbamoyl)-2-(thiophen-2-yl)ethyl)carbamic acid tert-butylesterHCID 10494327—
SolventDichloromethaneHCID 6344—
Product(2R)-N-methyl-2-methylamino-3-(thiophen-2-yl)propionamideHCID 1053597390.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Methyl-N-((1R)-1-(methylcarbamoyl)-2-(thiophen-2-yl)ethyl)carbamic acid tert-butylester (1.17 g ; 3.92 mmol) was dissolved in methylene chloride (4 ml). The reaction was cooled to 0° C. and triflouroacetic acid was added. The mixture was stirred at room temperature for 1.5 hour. Water (30 ml) and solid sodium hydrogencarbonate were added to pH 8. The phases were separated. The aqueous phase was extracted with methylene chloride (4×20 ml). The combined organic phases were dried over magnesium sulfate and the solvent was removed over vacuo to afford 0.70 g of (2R)-N-methyl-2-methylamino-3-(thiophen-2-yl)propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127391
Source datasetuspto-grants-2000_10
ORD IDord-2f817047872a4a34b7d55a0868506a49
Source noteuspto-grants-2000_10