Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 66612145 | HCID 66612145 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66611762 | HCID 66611762 | — |
Reaction Steps
Phenylmethyl 5-chloro-4-[(3,3-difluoro-1-pyrrolidinyl)carbonyl]-2-[(phenylmethyl)oxy]benzoate (may be prepared as described in Description 64; 444 mg, 0.92 mmol) was dissolved in tetrahydrofuran (4 ml) and LiOH (66.6 mg, 2.78 mmol) and water (1 ml) were added. The solution was heated at 45° C. for 90 minutes. 2M Hydrochloric acid (1.39 ml, 2.78 mmol) was added and the solvent was removed in vacuo. The solid was partitioned between 2M HCl (5 ml) and ethyl acetate (40 ml), and the organic layer separated, dried (MgSO4) and the solvent removed in vacuo to give the title compound as a brown solid. 374 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365551B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-cec5d6b832744b2d95708759a9e78d71 |
|---|
| Source note | uspto-grants-2016_06 |
|---|