Ethanol → 3-Bromo-5-[(1S)-2-tert-butoxy-1-methylethoxy]benzoic acid

To a stirred solution of 3-bromo-5-[(1S)-2-tert-butoxy-1-methylethoxy]benzonitrile (1.00 equiv, 42.60 mmoles, 13.30 g) in ethanol (135 mL) and water (13.30 mL) was added sodium hydroxide liquor (46/48% w/w, 5213.0 mmol, 12.10 mL, 18.27 g). The resultant yellow solution was heated to reflux for 1 hour and the solvent removed in vacuo to give a wet orange solid. The mixture was partitioned between water (150 mL) and MTBE (100 mL). The coloured upper organic phase contained two layers and was separated from the lower aqueous phase. Note: high solubility of the product sodium salt in the organic phase; only minor loss to the aqueous layer. The organic layers were concentrated to give a gummy orange solid (approx 18 g). The residue was partitioned between aqueous HCl (1M, 200 mL) and MTBE (150 mL). The Layers were separated and the aqueous phase further extracted with MTBE (100 mL). The organic phases were combined, washed with saturated brine (100 mL), dried over MgSO4, filtered and concentrated in vacuo to give an orange gum (12.85 g), which solidified on standing.

1. temperatureThe resultant yellow solution was heated
2. temperatureto reflux for 1 hour
3. customthe solvent removed in vacuo
4. customto give a wet orange solid
5. customThe mixture was partitioned between water (150 mL) and MTBE (100 mL)
6. customwas separated from the lower aqueous phase
7. concentrationThe organic layers were concentrated

ORD record

ord-4b79c083a561463f894c66d70174c782

Source dataset

uspto-grants-2011_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07973178B2