HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750437Generated: October 31, 2026
N,N-Dimethylbenzamide → 2-Thiophenecarboxylic acid
https://huagongshe.com/reaction/750437
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylbenzamide | HCID 11916 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Thiophenecarbonitrile | HCID 66087 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Thiophenecarboxylic acid | HCID 10700 | — |
| Product | 2-Thiophenecarboxamide | HCID 22063 | — |
Reaction Steps
To a 15-mL polypropylene centrifuge tube was added 3.86 mL of 50 mM potassium phosphate buffer (pH 7.0), 1.0 mL of a suspension of 22.1 mg dry cell weight E. coli SW132 wet cells (prepared as described in Example 10) in 50 mM potassium phosphate buffer (pH 7.0), and 0.1691 g of 2-thiophenecarbonitrile. The final concentration of 2-thiophencarbonitrile was 0.307 M. The reaction mixture was mixed on a rotating platform at 27° C. After 30 min, 7.50 mL of 95:5 acetonitrile/water containing 0.30 M N,N-dimethylbenzamide (HPLC external standard) was added to the reaction, the resulting mixture centrifuged, and a 0.100 mL of the supernatant mixed with 0.900 mL of acetonitrile and analyzed by HPLC. The conversion of 2-thiophenecarbonitrile was 99.5%, and the yields of 2-thiophenecarboxamide and 2-thiophenecarboxylic acid were 98% and 0%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405064B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-bcf9deda78ac4f65afa391c60b6674e3 |
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| Source note | uspto-grants-2008_07 |
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