HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylphenol → 2-(Biphenyl-3-yloxymethyl)-thiazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylphenol | HCID 11381 | — |
| Reactant | Ethyl 2-(bromomethyl)-1,3-thiazole-4-carboxylate | HCID 11043146 | — |
| Product | 2-(Biphenyl-3-yloxymethyl)-thiazole-4-carboxylic acid | HCID 11243864 | — |
Reaction Steps
2-(Biphenyl-3-yloxymethyl)-thiazole-4-carboxylic acid was prepared using general procedure B from 3-phenylphenol (available from Aldrich, Milwaukee, Wis.) and 2-bromomethyl-thiazole-4-carboxylic acid ethyl ester (Intermediate 3). Yield: 65 mg. Mass spectrum (ES) MH+=312.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700632B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-e887853d3d9341c1ae4f9edb0fa711ce |
| Source note | uspto-grants-2010_04 |