HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl bromoacetate → HCID 12135274, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | HCID 12135273 | HCID 12135273 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 12135274 | HCID 12135274 | — |
Reaction Steps
This compound was prepared from (2-benzyl-benzofuran-3-yl)-(3,5-diiodo-4-hydroxy-phenyl)-methanone and tert-butyl bromoacetate in substantially the same manner, as described in Example 2. Formic acid was used in the place of trifluoroacetic acid. The product was obtained as an off-white solid, mp 144-146° C.; MS m/e 638 (M+); Analysis for: C24H16I2O5Calc'd: C, 45.17; H, 2.53 Found: C, 44.19; H, 2.42
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166069 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-477fa23192f94779811c604345b4b4dc |
| Source note | uspto-grants-2000_12 |