HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-Chloro-4-(1-indolinylcarbonylamino)phenylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate | HCID 17859294 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-Chloro-4-(1-indolinylcarbonylamino)phenylacetic acid | HCID 17858863 | 60.4% |
Reaction Steps
To ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate (3.07 g, 8.56 mmol) were added 0.25N NaOH (68.4 ml, 17.1 mmol) and THF (70 ml). The mixture was heated and refluxed for 4 hours. After cooling, the reaction mixture was poured in 1N hydrochloric acid (50 ml). The crystals thus precipitated were collected by filtration, and dried under reduced pressure for 12 hours, whereby 3-chloro-4-(1-indolinylcarbonylamino)phenylacetic acid (1.71 g, 60%) was obtained as a colorless crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157487B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-bc9fae70bf514bc6a664cab11690dfa2 |
| Source note | uspto-grants-2007_01 |