Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86748116 | HCID 86748116 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86748115 | HCID 86748115 | 84.4% |
Reaction Steps
(Z)-alpha-(methoxyimino)-5-[2-(2-naphthalenyloxy)ethoxy]-2-thiopheneacetic acid ethyl ester (0.2 g) in methanol (2 mL) and tetrahydrofuran (2 mL) was treated with 3N sodium hydroxide (0.5 mL) and the stirred mixture was heated at 50° C. for 30 minutes. After the solvents were removed in vacuo, the concentrate was diluted with water (10 mL), acidified with 1N hydrochloric acid (3 mL) and extracted with dichloromethane (2×10 mL). The combined organic layers were washed with brine, dried (MgSO4) and evaporated. The resulting solid was crystallized from dichloromethane-hexane to provide 0.157 g of (Z)-alpha-(methoxyimino)-5-[2-(2-naphthalenyloxy)ethoxy]-2-thiopheneacetic acid as its hernihydrate, mp 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344843 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-c26fbf492ab148c0a8cbf41fee838f4d |
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| Source note | uspto-grants-1994_09 |
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