HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 4,6,Dichlorotryptophan ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 2-(hydroxyimino)-3-(4,6-dichloro-3-indolyl)propanoate | HCID 73607732 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4,6,Dichlorotryptophan ethyl ester | HCID 22857601 | 98% |
Reaction Steps
Dissolve ethyl 2-(hydroxyimino)-3-(4,6-dichloro-3-indolyl)propanoate (1.10 g, 3.65 mmol) in acetic acid (200 mL) and add activated zinc dust (1.25 g, 19.2 mmol). Stir at room temperature for 72 hours. Evaporate the acetic acid in vacuo to give a white oil. Take the white oil up in ethyl acetate (200 mL) and treat with saturated sodium hydrogen carbonate (500 mL). Filter the resulting white precipitate and separate the organic phase. Wash with saturated sodium hydrogen carbonate (100 mL) and brine (100 mL). Dry (MgSO4) and evaporate the solvent in vacuo to give the title compound as an amber oil (1.02 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05470870 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-c0cf8d2406ff46008d9606c47023eb33 |
| Source note | uspto-grants-1995_11 |