HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-N-Boc-Amino-Thiazole-5-Carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-((tert-butoxy(hydroxy)methylidene)amino)-1,3-thiazole-5-carboxylate | HCID 7213140 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-N-Boc-Amino-Thiazole-5-Carboxylic Acid | HCID 22271442 | 101% |
Reaction Steps
To a vigorously stirred suspension of ethyl 2-(tert-butoxycarbonylamino)thiazole-5-carboxylate (4.2 g, 15 mmol) in methanol (11 mL) was added 2 M aqueous solution of NaOH (22 mL, 44.0 mmol). The suspension was stirred at room temperature overnight. The mixture was concentrated in vacuo to remove methanol. The residual aqueous suspension was acidified with 6 N aqueous solution of HCl to pH ˜1-2. The mixture was stirred and occasionally sonicated for 1 hr. The solid was filtered, washed with water, and dried to give 2-(tert-butoxycarbonylamino)thiazole-5-carboxylic acid (3.7 g, 100% yield) as a white solid. MS found: (M+H-Boc)+=145.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304539B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-09a7564e41b348dd8398446661c3ba65 |
| Source note | uspto-grants-2012_11 |