HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → 1-Benzyloxycarbonyl-5-chloro-3-formylindol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-chloro-1H-indole-3-carbaldehyde | HCID 2795374 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyloxycarbonyl-5-chloro-3-formylindol | HCID 18473987 | — |
Reaction Steps
To a solution of 5-chloro-3-formylindole (5.00 g) in tetrahydrofuran (135 ml) was added sodium hydride (60% oil suspension, 3.53 g). The mixture was stirred for 20 minutes at room temperature. Carbobenzoxychloride (6.64 ml) was added to the mixture. After being stirred for 1 hour at room temperature, the whole was poured into ice water. The mixture was extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate. The solution was concentrated to give a residue, which was subjected to silica gel chromatography. Elution with hexane-ethyl acetate (5:1) provided 1-benzyloxycarbonyl-5-chloro-3-formylindol (5.74 g) as a crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06414003B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-8f5c9c6849e442b09051d7787c265e50 |
| Source note | uspto-grants-2002_07 |