HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 88627177, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 88627012 | HCID 88627012 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 88627177 | HCID 88627177 | — |
Reaction Steps
Ethyl 2-(2-aminothiazol-4-yl)-(Z)-2-(trans-2-methoxycyclohexyloxyimino)acetate (1.79 g) was hydrolysed with IM sodium hydroxide (10.75 ml) in ethanol (20 ml) as described in Example 4e. After acidification of the aqueous phase to pH 2-3 the water was removed under reduced pressure. The residue was extracted with hot ethanol and concentrated to dryness to give a brown foam. Trituration with ethyl acetate gave the title compound as a buff coloured solid (0.904 g). νmax (KBr) 3302, 3207, 1628, 1534, and 1450 cm-1 ; δH ((CD3)2SO) inter alia 1.00-2.00 (8H, m), 3.00-3.33 (4H, m and s), 3.90-4.30 (1H, m), 6.87 (1H, s), and 7.28 (3H, br. s). [Mass spectrum: +ve ion (thioglycerol) MH+ (300), MNa+ (322)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816452 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-47d8a4af65d042f79067fee8da71f708 |
| Source note | uspto-grants-1989_03 |