HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 59451365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 86761644 | HCID 86761644 | — |
| Product | HCID 59451365 | HCID 59451365 | — |
Reaction Steps
To a solution of 1-(1,1-dimethylethyl)2-ethyl 5-({2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethyl}oxy)-1H-indole-1,2-dicarboxylate (167 mg, 0.385 mmol) in MeOH (2 mL) was added 1N LiOH (0.58 mL). A precipitate appeared and THF (2 mL) was added. The solution was stirred until TLC showed the starting material had been consumed. The reaction mixture was quenched with 1N HCl (0.58 mL) and the solvent evaporated. The residue was dissolved in EtOAc and extracted with 1N NaOH. The aqueous layer was acidified with conc. HCl until a precipitate formed and then partitioned with EtOAc. The organic layer was separated, dried over MgSO4 and the solvent evaporated. The crude material was directly with no further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-1d30dfccf0764516a2fb5b7b8c682f7a |
| Source note | uspto-grants-2012_11 |