HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 53940535, compound → HCID 21426445, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 53940535 | HCID 53940535 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 21426445 | HCID 21426445 | 60.2% |
Reaction Steps
Ethyl (2-methylthio-imidazol-1-yl)-acetate (14.5 g.) in 4 N sulphuric acid (30 cc.) is heated under reflux for 1 hour. The sulphate ions are then removed by adding an aqueous solution of barium hydroxide and filtering off the precipitated barium sulphate. The filtrate is treated with decolorising charcoal and is then concentrated to dryness under reduced pressure (20 mm.Hg). The residue is taken up in benzene (80 cc.) and the mixture is again concentrated to dryness under reduced pressure (20 mm.Hg); this step is then repeated. Purification of the product by recrystallisation from dimethylformamide (30 cc.) yields (2-methylthio-imidazol-1-yl)-acetic acid (7.5 g.), m.p. 176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04034088 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-35f125855483496fa6611390265065df |
| Source note | uspto-grants-1977_07 |