HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → Ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate | HCID 67107394 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoate | HCID 67108192 | 73.8% |
Reaction Steps
Boron tribromide (1M solution in DCM, 5.85 ml) was added dropwise to a stirred, cooled solution of ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 61, 2.3 g) in dry DCM (45 ml) at −70° C. The resultant mixture was stirred at −70° C. for 40 minutes, then allowed to warm to room temperature. It was stirred at room temperature for 2 hours then poured into sodium bicarbonate (saturated aqueous solution). The layers were separated and the aqueous layer was extracted with further DCM. The combined organic layers were washed with brine, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness to give ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoate (1.64 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067905B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-9b388b3b5dff40f0b2e05f1f08aa39c7 |
| Source note | uspto-grants-2015_06 |