HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → cis-2-(Thiophen-2-ylmethoxycarbonylamino)-cyclohexanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | trans-2-Aminocyclohexanecarboxylic acid | HCID 2724640 | — |
| Reactant | 4-Nitrophenyl thiophen-2-ylmethyl carbonate | HCID 69761564 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | cis-2-(Thiophen-2-ylmethoxycarbonylamino)-cyclohexanecarboxylic acid | HCID 70133397 | — |
Reaction Steps
To a solution of Trans-2-amino-1-cyclohexane carboxylic acid (100 mg, 0.7 mmol) in 1 mL of water is added 2M aqueous Na2CO3 until pH=9-10 (2 mL). A solution of the carbonic acid 4-nitro-phenyl ester thiophen-2-ylmethyl ester (195 mg, 0.7 mmol) in THF (1 mL) is added at 0° C. and, after 10 minutes, 1 ml of the 2M Na2CO3 is added to the reaction. The mixture is allowed to warm to RT and vigorously stirred overnight. The reaction mixture is diluted with 0.5N HCl until pH=4-3 and the water layer is extracted three times with CH2Cl2 (10 ml). The organic phases are combined, dried (MgSO4), and concentrated under reduced pressure. The resulting product is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462076B2 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-65fce32f75f242149119773b48a59664 |
| Source note | uspto-grants-2002_10 |