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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567897Generated: October 30, 2026

2,2-Dimethoxypropane → HCID 86756341, compound

https://huagongshe.com/reaction/567897

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DimethoxypropaneHCID 6495—
Reactantethyl 2-amino-5-benzylthiophene-3-carboxylateHCID 3792137—
ReactantSodium borohydrideHCID 4311764—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 86756341HCID 86756341—

Reaction Steps

To a solution of 2-amino-5-(phenylmethyl)thiophene-3-carboxylic acid, ethyl ester (2.61 g) and 4-methylbenzenesulfonic acid (30mg) in dry toluene (50 ml) was added 2,2-dimethoxypropane. The solution was heated to reflux for 5 hours and then allowed to cool to ambient temperature. A solution of sodium borohydride (800 mg) in ethanol (100 ml) was added to the solution and the mixture was stirred at room temperature under nitrogen for 24 hours. The mixture was diluted with water and then extracted thrice with ethyl acetate. The combined organic extracts were washed with brine and then dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure to give an oil. The residue was purified by column chromatography over silica, eluting with diethyl ether:isohexane (1:19) to give the subtitle compound (550 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180635B2
Source datasetuspto-grants-2001_01
ORD IDord-12e33d0101b04236bb0405962bdc5ff5
Source noteuspto-grants-2001_01