HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (2-Amino-5-bromo-3-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-5-bromo-3-methoxybenzoic acid | HCID 45480457 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Amino-5-bromo-3-methoxyphenyl)methanol | HCID 46738297 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2-amino-5-bromo-3-methoxybenzoic acid (20.0 g, 81.30 mmol) is suspended in 250 mL THF, cooled to 0° C. and combined with borane-THF complex (315 mL, 0.315 mol). The reaction mixture is stirred for 5 d at 20° C. and then combined with 10 mL EtOH, stirred for 15 min and then stirred into 250 mL water. The mixture is extracted 3× with DCM, the combined organic phases are dried and the solvent is eliminated in vacuo. The crude product is suspended in DCM and extracted 2× with 400 mL 1 N hydrochloric acid. The combined aqueous phases are adjusted to pH 5-6 with potassium carbonate, the precipitate formed is filtered off and (2-amino-5-bromo-3-methoxy-phenyl)-methanol (HPLC-MS: tRet.=1.41 min, MS(M+H)+=232/234; method FEC3) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637549B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-1d642fcfe5fa48daa9ad3998695a57e1 |
| Source note | uspto-grants-2014_01 |