Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908231Generated: October 29, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-(Trifluoromethyl)benzo[b]thiophene

https://huagongshe.com/reaction/1908231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acidHCID 2783043—
SolventHydrochloric AcidHCID 313—
SolventDimethylacetamideHCID 31374—
Product5-(Trifluoromethyl)benzo[b]thiopheneHCID 1174569974.3%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 5-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid (2.00 g, 8.12 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (5.0 mL, 34 mmol) in DMA (13 mL) was heated via microwave irradiation at 200° C. for 1 h. The reaction was cooled to rt, diluted with HCl (1 N aq., 20 mL) and extracted with EtOAc (20 mL). The organic layer was washed with water (10 mL), dried (Na2SO4) and concentrated. The residue was taken up in Et2O (25 mL) and washed with water (25 mL). The aqueous layer was extracted with Et2O (10 mL×2). The combined Et2O layers were dried (Na2SO4) and concentrated. The crude material was purified (FCC) to yield the title compound (1.22 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598202B2
Source datasetuspto-grants-2013_12
ORD IDord-0c323f83306e40089a78efb900a26d77
Source noteuspto-grants-2013_12