HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 18433429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 22728151 | HCID 22728151 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18433429 | HCID 18433429 | — |
Reaction Steps
N-Cyclobutyl-5-(2,6-dimethyl-4-nitro-phenoxy)-2-hydroxy-N-methyl-benzamide was prepared from N-cyclobutyl-5-(2,6-dimethyl-4-nitro-phenoxy)-2-methoxy-N-methyl-benzamide according to a procedure analogous to that described in EXAMPLE 2, Step B. Boron tribromide (1M in dichloromethane, 2.0 equiv) was used. After water addition, the mixture was extracted with dichloromethane (3×10 ml). The combined organic phases were dried over anhydrous Na2SO4, filtered, and concentrated. The title product of Step E was used in the next step without purification. MS (APCI+) Calc.: 370.4, Found: 371.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441015B2 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-c06604e91acc40abb1c32d870a120a5b |
| Source note | uspto-grants-2002_08 |