HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462052Generated: November 1, 2026
Trifluoroacetic acid → HCID 53647970, compound
https://huagongshe.com/reaction/1462052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzo(B)Thiophene | HCID 7221 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 13318579 | HCID 13318579 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53647970 | HCID 53647970 | 88% |
Reaction Steps
A solution of 5.15 g. (29.4 mM) of DL N-allyloxycarbonyl-α-hydroxyglycine and 3.95 g. (29.4 mM) of benzo[b]thiophene in 40 ml. of trifluoroacetic acid was stirred at 22.5° C. for eighteen hours. The reaction mixture was then concentrated by evaporation under reduced pressure to give an oil, and the oil was dissolved in a mixture of 100 ml. of ethyl acetate and 100 ml. of water. The organic layer was separated, and the aqueous layer was extracted twice more with 50 ml. portions of fresh ethyl acetate. The organic extracts were combined, washed with water, and then extracted twice with 100 ml. portions of 10% aqueous sodium bicarbonate. The aqueous extracts were combined, added to 100 ml. of fresh ethyl acetate, and acidified to pH 2.0 by the addition of conc. hydrochloric acid. The organic layer was separated and the aqueous acid layer was extracted with two 50 ml. portions of fresh ethyl acetate. The organic portions were combined, dried, and the solvent was removed by evaporation to provide 7.55 g. (88% yield) of N-allyloxycarbonyl-(3-benzothienyl)glycine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04458085 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-275d06662cf8468ebbc18575da29140c |
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| Source note | uspto-grants-1984_07 |
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