HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydroxide, monohydrate → 4'-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 4'-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid methyl ester | HCID 57851121 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid | HCID 57851511 | 93% |
Reaction Steps
A solution of LiOH.H2O (1.86 g, 44.2 mmol) in H2O (40 mL) was added dropwise to a suspension of 4′Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid methyl ester (10 g, 34 mmol) in THF (25 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and was stirred until the reaction solution turned clear. Solvent was removed under vacuum and the aqueous solution was acidified by addition of 10% HCl to pH=3. The resulting precipitate was collected and dried to afford 4′-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid as white solid (8.85 g, 93%). MS (M+H)=281.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846945B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-b859851a9b784d41ab36de0c22987a8b |
| Source note | uspto-grants-2014_09 |