HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 6-Chloro-5-hydroxy-1H-indole-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | ethyl 6-chloro-5-methoxy-1H-indole-2-carboxylate | HCID 12200732 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-5-hydroxy-1H-indole-2-carboxylic acid ethyl ester | HCID 67017914 | 74.6% |
Reaction Steps
To a cooled (−78° C.) solution of 6-chloro-5-methoxy-1H-indole-2-carboxylic acid ethyl ester (930 mg, 1.0 eq.) in dichloromethane (20 mL), was slowly added a 1M solution of boron tribromide in dichloromethane (7.33 mL, 2.0 eq.). The mixture was stirred at room temperature for 1 h, partitioned between ethyl acetate and ice water. The aqueous layer was extracted with ethyl acetate and the combined organic fractions were washed with 10% sodium bicarbonate solution and brine, dried over sodium sulfate, filtered, evaporated to dryness and purified on silica gel, eluting with a 4:1 to 3:1 gradient of cyclohexane/ethyl acetate, to yield 655 mg (74%) of the title compound as a light-brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507736B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-2fa291c04abe4df0ac9941ccc6fda1bc |
| Source note | uspto-grants-2009_03 |