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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73168Generated: October 25, 2026

Acetic Acid → Methyl 3-(isopropyl-amino)-5-phenylthiophene-2-carboxylate

https://huagongshe.com/reaction/73168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-MethoxypropeneHCID 8300—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-(isopropyl-amino)-5-phenylthiophene-2-carboxylateHCID 1173744796.4%

Reaction Steps

To a stirred solution of 3-Amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (1.82 g, 7.8 mmol) in 1,2-dichloroethane (40 mL) was added sequentially 2-methoxypropene (3.0 mL, 31.2 mmol), AcOH (1.8 mL, 31.2 mmol) and NaBH(OAc)3 (3.31 g, 15.6 mmol) and stirred for 2 hrs. It was then diluted with EtOAc and H2O. The aqueous solution was adjusted to pH=7 by adding NaHCO3. The aqueous phase was extracted with EtOAc, the combined extract was washed with brine and dried on MgSO4 and filtered. Purification on bond elute with hexane to 5% EtOAc-hexane furnished 3-Isopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester (2.07 g, 96% yield). 1H NMR (CDCl3, 400 MHz): δ 7.62 (d, 2H), 7.40 (m, 3H), 6.91 (s, 1H), 3.84 (s, 3H), 3.71 (m, 1H), 1.35 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829030B2
Source datasetuspto-grants-2014_09
ORD IDord-7eca7fdfe5a54abb85fa03b7ac19f993
Source noteuspto-grants-2014_09