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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747035Generated: November 1, 2026

Water → HCID 58009627, compound

https://huagongshe.com/reaction/1747035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDi-tert-butyl IminodicarboxylateHCID 279800—
ReactantMethyl 5-(chloromethyl)thiophene-3-carboxylateHCID 12926494—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58009627HCID 5800962783.5%

Reaction Steps

To a solution of 3.69 g of di-tert-butyl imidodicarbonate in 54 ml of DMF was added 1.91 g of potassium tert-butoxide at 0° C. under argon, followed by stirring at room temperature for 1 hour. A solution of 2.7 g of methyl 5-(chloromethyl)thiophene-3-carboxylate in 8.1 ml of DMF was slowly added thereto, followed by stirring at room temperature overnight. Water and ethyl acetate were added to the reaction solution, followed by carrying out an extraction operation, and the organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain 4.394 g of methyl 5-{[bis(tert-butoxycarbonyl)amino]methyl}thiophene-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150541B2
Source datasetuspto-grants-2015_10
ORD IDord-77cd3f4bc95d444fa80b73f16faa96cd
Source noteuspto-grants-2015_10