Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethylacetamide | HCID 12253 | — |
| Reactant | (E)-2-Methyl-2-butenenitrile | HCID 5355732 | — |
| Reactant | cis-2-Methyl-2-butenenitrile | HCID 6028739 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | Tiglic acid | HCID 125468 | — |
| Product | 2,3-Dimethylacrylic acid, (Z)- | HCID 643915 | — |
Reaction Steps
A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture containing 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0), 38.4 mg of (E)-2-methyl-2-butenenitrile (47.4 mM final concentration of (E)-2-methyl-2-butenenitrile), and 37.7 mg of (Z)-2-methyl-2-butenenitrile (46.5 mM final concentration of (Z)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 25° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 23 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220562B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-47d6acf0726a4877a66d87005b159381 |
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| Source note | uspto-grants-2007_05 |
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