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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352183Generated: October 25, 2026

Methanol → Tiglic acid

https://huagongshe.com/reaction/1352183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetonitrileHCID 6342—
ReactantEthylacetamideHCID 12253—
Reactant(E)-2-Methyl-2-butenenitrileHCID 5355732—
Reactantcis-2-Methyl-2-butenenitrileHCID 6028739—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductTiglic acidHCID 125468—
Product2,3-Dimethylacrylic acid, (Z)-HCID 643915—

Reaction Conditions

Temperature35 °C

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 4.80 mL of 50 mM potassium phosphate buffer (pH 7.0), 80.5 mg of (E)-2-methyl-2-butenenitrile (100 mM final concentration of (E)-2-methyl-2-butenenitrile), and 80.7 mg of (Z)-2-methyl-2-butenenitrile (100 mM final concentration of (Z)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 35° 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 6 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 99% and 0%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220562B2
Source datasetuspto-grants-2007_05
ORD IDord-8254a10ef4c74add97c747df4942c44e
Source noteuspto-grants-2007_05