HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 5-(bromomethyl)thiophene-2-carboxylate → HCID 11314240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 5-(bromomethyl)thiophene-2-carboxylate | HCID 11424851 | — |
| Reactant | 4-Hydroxy-2'-nitrobiphenyl | HCID 15541112 | — |
| Product | HCID 11314240 | HCID 11314240 | — |
Reaction Steps
5-(2′-Nitro-biphenyl-4-yloxymethyl)-thiophene-2-carboxylic acid was prepared using general procedure A from 4-hydroxy-2′-nitrobiphenyl (available from TCI America, Portland, Oreg.) and 5-bromomethyl-thiophene-2-carboxylic acid methyl ester (Intermediate 7). Yield: 80 mg. Mass spectrum (ES) MH+=356.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07355049B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-ac0e8462c19649c58b269b9c3eec2ed2 |
| Source note | uspto-grants-2008_04 |