Boron tribromide → 2,6-Dichloro-3,4-dihydroxybenzaldehyde

温度

-65 °C

Into an oven-dried, three-neck round bottom flask, fitted with a thermometer, 1.0 g (4.52 mmol; Aldrich, Milwaukee, Wis.) of 2,6-dichloro-3-hydroxy-4-methoxybenzaldehyde and 45 mL of dichloromethane were added under nitrogen atmosphere. The solution was cooled to −65° C. and 1.32 mL (14 mmol) of boron tribromide was added dropwise. The reaction mixture was left to warm up slowly to room temperature with stirring for 16 hours. The reaction mixture was carefully quenched with the addition of 5 mL of water, then transferred to a single-neck round bottom flask and volatiles were removed in vacuo. The residue was taken up with 50 mL of ethylacetate and washed three times with water and two times with brine. The organic layer was dried over MgSO4, then concentrated to yield 0.9 g (96%) of crude 2,6-dichloro-3,4-dihydroxybenzaldehyde, as an off-white solid, which was used without further purification. 1H-NMR δ (d6-acetone): 6.85 (1H, s), 9.1 (2H, br s), 10.2 (1H,s). Melting point=213-215° C.

1. additionwere added under nitrogen atmosphere
2. waitThe reaction mixture was left
3. temperatureto warm up slowly to room temperature
4. customThe reaction mixture was carefully quenched with the addition of 5 mL of water
5. customtransferred to a single-neck round bottom flask
6. customvolatiles were removed in vacuo
7. washwashed three times with water and two times with brine
8. dry with materialThe organic layer was dried over MgSO4
9. concentrationconcentrated

ORDレコード

ord-dbe945893e4147799822822281e1229e

出典データセット

uspto-grants-2009_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07638036B2