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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133497Generated: October 25, 2026

1,1,1-Trifluoro-2,4-pentanedione → 2,2,2-Trifluoro-1-(2-methyl-4-thiophen-2-yl-5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-b]pyridin-3-yl)-ethanone

https://huagongshe.com/reaction/133497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluoro-2,4-pentanedioneHCID 73943—
Reactant(2-Amino-4,5,6,7-tetrahydro-1-benzothien-3-yl)(thien-2-yl)methanoneHCID 2535023—
CatalystSulfuric AcidHCID 1118—
SolventAcetic AcidHCID 176—
Product2,2,2-Trifluoro-1-(2-methyl-4-thiophen-2-yl-5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-b]pyridin-3-yl)-ethanoneHCID 1150918423.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 50 mg (0.19 mmol) (2-amino-4,5,6,7-tetrahydro-benzo[b]thiophen-3-yl)-thiophen-2-yl-methanone in 1.5 ml acetic acid was added 0.024 ml (0.20 mmol) of 1,1,1-trifluoro-pentane-2,4-dione and one drop of sulfuric acid. The mixture was then stirred at 100° C. for 10 minutes in a microwave and then concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 9:1) afforded 17 mg (23%) 2,2,2-trifluoro-1-(2-methyl-4-thiophen-2-yl-5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-b]pyridin-3-yl)-ethanone as an orange oil. ES-MS m/e (%): 382 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390903B2
Source datasetuspto-grants-2008_06
ORD IDord-2450389431d6409cb2971bceac54a2c2
Source noteuspto-grants-2008_06