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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650184Generated: October 31, 2026

Acetic Acid → Ethyl 5-bromothiophene-2-carboxylate

https://huagongshe.com/reaction/1650184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CyanideHCID 8929—
Reactant5-Bromothiophene-2-carbaldehydeHCID 78428—
CatalystHCID 178418406HCID 178418406—
SolventEthanolHCID 702—
ProductEthyl 5-bromothiophene-2-carboxylateHCID 605723—

Reaction Steps

To 1.092 g (5.7157 mmol) of 5-bromothiophene-2-carboxaldehyde was added sequentially, 1.507 g (30.75 mmol) sodium cyanide, 60 ml ethanol, 602.5 mg (10.04 mmol) of acetic acid and 10.62 g (122.16 mmol) of manganese dioxide. This mixture was stirred at room temperature for 24 hours, then filtered through celite and the residue washed several times with ether. The combined filtrates were concentrated, then the residue taken up in water and extracted with 3×75 ml ether. Combined ether extracts were washed with saturated NaHCO3, saturated NaCl, dried (MgSO4), concentrated in vacuo and kugelrohr distilled (70° C.; 0.1 mm) to give the captioned compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923884
Source datasetuspto-grants-1990_05
ORD IDord-7ec0e38df6f04108a2865e6d16fab2ef
Source noteuspto-grants-1990_05