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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730989Generated: October 31, 2026

Acetic Acid → N-(7-Oxo-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)formamide

https://huagongshe.com/reaction/1730989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium ChlorideHCID 5234—
ReactantFormamide, N-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)-HCID 93944—
ProductN-(7-Oxo-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)formamideHCID 23347790—

Reaction Steps

A solution of N-formyl-4,5,6,7tetrahydrobenzo[b]thiophen-4-amine (60 g) in 50% aqueous acetic acid (1,112 ml) is stirred and ceric ammonium nitrate (727 g) is added over 20-25 minutes at 25° to 30° C. The mixture is stirred at room temperature for 15 minutes, saturated with sodium chloride and extracted with methylene chloride (2 × 770 and 1 × 400 ml). The combined methylene chloride extracts are washed with brine (380 ml) and then with water (155 ml). The water wash is extracted with methylene chloride (155 ml) and this extract is combined with the main methylene chloride extract. The methylene chloride is evaporated and the residue is triturated with ether (250 ml), collected and washed with ether to afford the title formamide, m.p. 104° to 110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994924
Source datasetuspto-grants-1976_11
ORD IDord-91b73b0f4d394ee2af1d41da62d389db
Source noteuspto-grants-1976_11