Phenol → Phenyl 3-methylbut-2-enoate

To an ice bath cooled solution of 1.29 g (54 mmol) of NaH (obtained from a 60% suspension in mineral oil by 3×10 ml hexane wash) in 20 ml of dry THF was added slowly under oxygen a solution of 5 g (53 mmol) of phenol in 50 ml of dry THF. The mixture was then treated with a solution of 7 g (59 mmol) of dimethylacryloyl chloride in 30 ml of dry THF. The cooling bath was then removed and the mixture was stirred for a further 2.5 h. The reaction mixture was then poured into 150 ml of water containing i ml of glacial acetic acid. The mixture was extracted with 150 ml ether and the ether extract washed with saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by flash chromatography (silica; 5% ether in hexanes) to give the title compound as a yellow oil. PMR (CDCl3)): & 1.99 (3H, s), 2.24 (3H, s), 5.93 (1H, broad s), 7.10 (2H, d, J-7.8 Hz) 7.22 (1H, t, J-7.8 Hz), 7.38 (2H, t, J-7.8 Hz). 4,4-Dimethyl-2-oxo-chroman (Compound 38)

1. washwash) in 20 ml of dry THF
2. customThe cooling bath was then removed
3. additionThe reaction mixture was then poured into 150 ml of water containing i ml of glacial acetic acid
4. extractionThe mixture was extracted with 150 ml ether
5. extractionthe ether extract
6. washwashed with saturated NaCl solution
7. dry with materialdried (MgSO4)
8. customThe solvent was removed in vacuo
9. customthe residue purified by flash chromatography (silica; 5% ether in hexanes)

ORD record

ord-af6bce520ed0455f8b34667944be70e3

Source dataset

uspto-grants-1997_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05616597