HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromocresol Green → HCID 54415452, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromocresol Green | HCID 6451 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-Oxo-undecanoic Acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl Ester | HCID 54155424 | — |
| Catalyst | Hydrochloride methanol | HCID 21893726 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54415452 | HCID 54415452 | 100.2% |
Reaction Steps
A solution of 10.00 g 4-oxo-undecanoic acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl ester was dissolved in 60 ml methanol and a trace of bromocresol green was added. When 1.63 g sodium cyanoborohydride was added, the color changed immediately from yellow to deep blue. Several drops of 2N HCl/methanol solution turned the color of the reaction back to yellow. The reaction was stirred for 2 ½ hours, with occasional addition of acid to maintain the yellow color. The reaction mixture was evaporated to dryness and water was added to the residue. This solution was extracted with ether and washed with water. The solution was dried, filtered and evaporated to dryness to yield 10.07 g of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06437150B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-b83402ba0af14c549f00ec16ec3b40b6 |
| Source note | uspto-grants-2002_08 |