HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → 1-Benzyloxycarbonyl-5-chloro-3-chloromethylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Benzyloxycarbonyl-5-chloro-3-hydroxymethylindole | HCID 18473921 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzyloxycarbonyl-5-chloro-3-chloromethylindole | HCID 18473963 | — |
Reaction Steps
To a solution of 1-benzyloxycarbonyl-5-chloro-3-hydroxymethylindole (1.45 g) in dichloromethane (23 ml) was added thionylchloride (0.797 μl) at −78° C. After the mixture was stirred for 1.5 hours at room temperature, the reaction mixture was concentrated under the reduced pressure to give a residue. Hexane was added to the residue. 1-benzyloxycarbonyl-5-chloro-3-chloromethylindole (1.43 g) was obtained as a crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06169102A |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-b0bfb1c87b064a4c936f2d06778c99b7 |
| Source note | uspto-grants-2001_01 |