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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505794Generated: November 4, 2026

Phosphoric Acid → methyl 5-(4-chlorophenyl)-6-cyclohex-1-en-1-yl-4H-thieno[3,2-b]pyrrole-2-carboxylate

https://huagongshe.com/reaction/505794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantAcetic AnhydrideHCID 7918—
ReactantCyclohexanoneHCID 7967—
Reactantmethyl 5-(4-chlorophenyl)-4H-thieno[3,2-b]pyrrole-2-carboxylateHCID 24976015—
SolventAcetic AcidHCID 176—
Productmethyl 5-(4-chlorophenyl)-6-cyclohex-1-en-1-yl-4H-thieno[3,2-b]pyrrole-2-carboxylateHCID 6846715391%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution (0.2 M) of methyl 5-(4-chlorophenyl)-4H-thieno[3,2-b]pyrrole-2-carboxylate in acetic acid was treated with acetic anhydride (2.5 eq.), cyclohexanone (10 eq.) and 85% phosphoric acid (2.1 eq.). The mixture was heated at 80° C. for 3.5 days. After cooling down it was poured into ice cold ammonium hydroxide. The product was extracted with AcOEt and the combined organic layers were washed sequentially with aqueous HCl (1 N), aqueous NaHCO, (saturated solution) and brine then dried and concentrated. The crude was purified by flash chromatography on silica gel (1:9 to 1:4 AcOEt/petroleum ether) affording the title compound (91%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781431B2
Source datasetuspto-grants-2010_08
ORD IDord-a441f15e86f544f48defa17382110b55
Source noteuspto-grants-2010_08