HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 4-(Biphenyl-4-ylmethoxycarbonylamino)-biphenyl-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-(Biphenyl-4-ylmethoxycarbonylamino)-biphenyl-3-carboxylic acid methyl ester | HCID 69686982 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Biphenyl-4-ylmethoxycarbonylamino)-biphenyl-3-carboxylic acid | HCID 22396283 | 63.5% |
Reaction Steps
To a solution of 4-(biphenyl-4-ylmethoxycarbonylamino)-biphenyl-3-carboxylic acid methyl ester (0.51 g, 1.179 mmol) in THF (5 mL) was added at room temperature 1.0 M LiOH (2.42 mL, 2.42 mmol) and the mixture was stirred for 3 h. The solvent was evaporated, water was added, followed by 2N HCl to adjust the pH to 1-2, and the product was extracted with ethyl acetate. The extract was washed with water, then brine, and dried over magnesium sulfate, concentrated to dryness and purified by chromatography to yield 0.317 g of 4-(biphenyl-4-ylmethoxycarbonylamino)-biphenyl-3-carboxylic acid 601, mp: 234.5-235.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06903086B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-c4fd0d99796b433796a834725d1d07ec |
| Source note | uspto-grants-2005_06 |