HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2-chlorobenzoic acid → (4-Bromo-2-chlorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2-chlorobenzoic acid | HCID 108829 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-2-chlorophenyl)methanol | HCID 43805739 | — |
Reaction Steps
To a stirring solution of 4-bromo-2-chlorobenzoic acid (11.1 g, 47 mmol) in THF (100 mL) at 0° C. under nitrogen was added borane-methyl sulfide complex (9.4 ml, 94 mmol) via syringe over 10 min. Gas evolution quite evident. Ice bath removed, and once gas evolution subsided reaction gently heated to reflux for 1 h. Reaction slowly quenched with MeOH (50 mL) and 2M HCl (20 mL). Aqueous extracted with 9:1 CHCl3/IPA (150 mL). Organic dried with sat NH4Cl, MgSO4, then concentrated to a colorless oil under reduced pressure. Product crystallized after 1 week sitting neat.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198448B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-8acfba3eb2b648d1bb72e6e12642ea26 |
| Source note | uspto-grants-2012_06 |