HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → HCID 69688505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | HCID 69688152 | HCID 69688152 | — |
| Product | HCID 69688505 | HCID 69688505 | 96.1% |
Reaction Steps
Ethyl 4-(S)-benzyloxycarbonylamino-4-cyclopropyl-2-butenoate was dissolved in dry nitromethane (15 ml), and the solution was mixed with 1,1,3,3-tetramethylguanidine (133 μl, 1.05 mol) and stirred at room temperature for 17 hours. The reaction solution was concentrated under a reduced pressure, the resulting residue was dissolved in chloroform (50 ml), and the solution was washed with 10% citric acid aqueous solution (50 ml) and saturated sodium chloride aqueous solution (50 ml) in that order, and then dried over anhydrous magnesium sulfate, thereby obtaining 1.207 g (96.1%) of the title compound as a yellow oil. This product (diastereomer mixture) was used in the subsequent reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06573260B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-48e1186bf58d4fae8ecc7b4d4f1d012d |
| Source note | uspto-grants-2003_06 |