Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86624422 | HCID 86624422 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59457499 | HCID 59457499 | 89% |
Reaction Steps
A mixture of 2-[4-(3-chloropropoxy)phenyl]-4-methyl-1,3-thiazole-5-carboxylate i105 (14.1 mmol, 1 eq, 4.6 g) and 2 M sodium hydroxide (28.2 mmol, 2 eq, 14.1 ml) in methanol (100 ml) is stirred at 70° C. overnight. The mixture is concentrated to dryness and taken up in a minimum of water. The aqueous phase is acidified by 1 N hydrogen chloride to reach pH 2 and poured into ice to afford precipitation of a white solid. The solid is filtered and dried under reduced pressure to give 3.9 g of 2-[4-(3-chloropropoxy)phenyl]-4-methyl-1,3-thiazole-5-carboxylic acid i106 as a white solid. This solid is used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790720B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-d5a05977c1364ee99a110d2eeb23d155 |
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| Source note | uspto-grants-2010_09 |
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