HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016474Generated: October 31, 2026
Sodium Hydroxide → 4-[2-(4-Tert-butoxycarbonylpiperazin-1-yl)thiazol-4-ylmethoxy]benzoic acid
https://huagongshe.com/reaction/1016474
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tert-butyl 4-(4-(4-methoxycarbonylphenoxymethyl)thiazol-2-yl]piperazine-1-carboxylate | HCID 18186636 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[2-(4-Tert-butoxycarbonylpiperazin-1-yl)thiazol-4-ylmethoxy]benzoic acid | HCID 18186513 | 100.9% |
Reaction Steps
A solution of tert-butyl 4-[4-(4-methoxycarbonylphenoxymethyl)thiazol-2-yl]piperazine-1-carboxylate (820 mg, 1.89 mmol) in methanol (30 mL) and THF (10 mL) was treated with a solution of sodium hydroxide (226 mg, 5.67 mmol) in water (10 mL). The mixture was stirred at 55° C. for 8 hours and then concentrated by evaporation. The aqueous solution was diluted with water (10 mL) and the dilution was acidified with dilute hydrochloric acid. A resulting solid was collected by filtration to provide 4-[2-(4-tert-butoxycarbonylpiperazin-1-yl)thiazol-4-ylmethoxy]benzoic acid (800 mg, 100% yield). HNMR (dmso-d6): 7.88 (2H, d), 7.09 (2H, d), 6.91 (1H, s), 4.99 (2H, s) 3.44 (8H, m), 1.41 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476026B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-bfcb996fd5f84bb3a974118e1e5066f1 |
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| Source note | uspto-grants-2002_11 |
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