HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 5-bromofuran-2-carboxylate → HCID 19744465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 5-bromofuran-2-carboxylate | HCID 599633 | — |
| Reactant | Methyl 5-bromopyridine-3-carboxylate | HCID 699336 | — |
| Reactant | (5-(thiophen-3-yl)pyridin-3-yl)methanol | HCID 11019666 | — |
| Reactant | Ethyl 5-bromothiophene-3-carboxylate | HCID 15293216 | — |
| Product | HCID 19744465 | HCID 19744465 | — |
Reaction Steps
When the same reaction as in Referential Example 59 is carried out except using 5-bromo-3-pyridine carboxylic acid methyl ester or 5-bromo-2-furancarboxylic acid methyl ester [J. Org. Chem., 21, 517 (1956)] instead of the starting 5-bromo-3-thiophenecarboxylic acid ethyl ester, 5-(3-thienyl)-3-pyridylmethanol or 5-(3-thienyl)-2-furylmethanol is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234946 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-f46971d7eda9469fabda5cf446036d05 |
| Source note | uspto-grants-1993_08 |