HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224902Generated: October 24, 2026
2-Thiopheneacetic acid → 2-[5-(Acetamidomethyl)thiophen-2-yl]acetic acid
https://huagongshe.com/en/reaction/224902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | Formicin | HCID 69365 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2-[5-(Acetamidomethyl)thiophen-2-yl]acetic acid | HCID 23330367 | — |
Reaction Steps
1.42 g of 2-thienylacetic acid are added in portions to a solution, kept at 0°-5° C., of 1.34 g of N-hydroxymethyl acetamide (Einhorn, Ann. Chem., volume 343, page 264 (1905)) in 10 ml of trifluoroacetic acid, whilst stirring. The mixture is stirred for 2 hours at 0°-5° C. and the trifluoroacetic acid is distilled off under reduced pressure. 30 ml of water are added to the residue and the mixture is extracted with twice 50 ml of ethyl acetate. The organic extracts are washed with a saturated aqueous sodium chloride solution, dried over magnesium sulphate, concentrated under reduced pressure and filtered through silica gel. The residue is crystallised from ethyl acetate and gives 2-(5-acetylaminomethyl-2-thienyl)-acetic acid, thin layer chromatogram (silica gel): Rf=0.61 (system: butanol/acetic acid/water, 45:45:10); infrared absorption spectrum (mineral oil): characteristic bands at 2.95μ, 5.82μ, 6.23μ and 6.38μ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04234578 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-7ab72f441ead46f0a1bceb54cbcbabec |
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| Source note | uspto-grants-1980_11 |
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