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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412407Generated: November 1, 2026

Benzo(B)Thiophene → HCID 53647970, compound

https://huagongshe.com/reaction/2412407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantHCID 13318579HCID 13318579—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53647970HCID 5364797088%

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 given 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492693
Source datasetuspto-grants-1985_01
ORD IDord-a73b9dc16ebe4aa58ef693c489089a0f
Source noteuspto-grants-1985_01