Phenol → HCID 86710600, compound

Temperature

60 °C

Following GENERAL METHOD 5-1 for phenol alkylation, Cs2CO3 (485 mg, 1.489 mmol) was added to a solution of 7-(benzyloxy)-6-bromonaphthalen-2-ol (490 mg, 1.489 mmol) in acetone (14.90 mL) at RT. The reaction mixture was stirred for 5 min then ((3-bromopropoxy)methyl)benzene (682 mg, 2.98 mmol) was added, followed by addition of NaI (446 mg, 2.98 mmol). The reaction mixture was heated to 60° C. and stirred overnight, then filtered, washed with acetone and concentrated in vacuo. The resulting residue was partitioned between Et2O (60 mL) and water (20 mL). After separation, the organic layer was washed with saturated aq. sodium sulfite solution (20 mL), 2 M Na2CO3, and brine. The organic layer was then dried over MgSO4, filtered, and concentrated in vacuo. Silica gel chromatography (10-60% EtOAc/heptane) afforded 3-(benzyloxy)-6-(3-(benzyloxy)propoxy)-2-bromonaphthalene (422 mg, 0.884 mmol, 60% yield) as a white solid (eluting at 30% EtOAc). LCMS Rt=1.81 min (condition C); LCMS (M+1)=479.9.

1. stirringstirred overnight
2. filtrationfiltered
3. washwashed with acetone
4. concentrationconcentrated in vacuo
5. customThe resulting residue was partitioned between Et2O (60 mL) and water (20 mL)
6. customAfter separation
7. washthe organic layer was washed with saturated aq. sodium sulfite solution (20 mL), 2 M Na2CO3, and brine
8. dry with materialThe organic layer was then dried over MgSO4
9. filtrationfiltered
10. concentrationconcentrated in vacuo
11. customSilica gel chromatography (10-60% EtOAc/heptane) afforded

ORD record

ord-30b2cd6d0bc647359469a82493569f6d

Source dataset

uspto-grants-2014_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08729263B2