HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bismuth trichloride → HCID 68992465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bismuth trichloride | HCID 24591 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | HCID 14096412 | HCID 14096412 | — |
| Reactant | HCID 68994234 | HCID 68994234 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68992465 | HCID 68992465 | — |
Reaction Steps
A 82.6 g quantity of 6,6-dibromo-2,2-dimethylpenam-3-carboxylic acid 1-oxide p-nitrobenzyl ester (Compound 4) [compound of the formula (1) wherein X═Y═Br, R=p-nitrobenzyl, n=1] was dissolved in 300 mL of dichloromethane. To the solution was added 115 mL of 20% aqueous solution of ammonium chloride and 36 mL of methanol with stirring. After adding 1.6 g of bismuth chloride and 10 g of aluminum powder at one time, the mixture was reacted at 40° C. for 8 hours. An organic layer was separated and concentrated by an evaporator to give 6-bromo-2,2-dimethylpenam-3-carboxylic acid 1-oxide p-nitrobenzyl ester (Compound 5) [compound of the formula (1b) wherein X═Br, Y═H, R=p-nitrobenzyl, n=1] in a yield of 65%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514553B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-e74d3d2db1b343989c3bbbd1f5346907 |
| Source note | uspto-grants-2009_04 |