تفاعل #90241
ord-0eaedb2a6a374ed7832cad69cb530dc5
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىTo prepare 22
- 2استخلاصThe mixture was extracted twice with hexanes (15 ml)
- 3غسيلThe organic phase was washed twice with water (15 ml)
- 4تجفيفdried over Na2SO4
- 5تركيزconcentrated in vacuum
- 6workup.DISSOLUTIONThe residue (3.7 g) was dissolved in THF (10 ml)
- 7workup.ADDITIONtreated with water (7 ml) and glacial acetic acid (21 ml)
- 8workup.ADDITIONthe mixture was added to ice water
- 9استخلاصextracted twice with a 1:1 mixture (v/v) of diethyl ether and hexanes (30 ml)
- 10غسيلThe organic phase was washed with water (30 ml)
- 11تجفيفdried over Na2SO4
- 12تركيزconcentrated in vacuum
الإجراء التجريبي
To prepare 22, a solution of 4-hydroxybenzoic acid (21, 1.52 g, 10 mmol) in DMF (7 ml) was treated with DIPEA (5.2 ml, 30 mmol) and tert-butyldimethylsilyl chloride (3.7 g, 24.5 mmol). After 12 hours, the mixture was brought to a pH of 4 by addition of 1 M H3PO4. The mixture was extracted twice with hexanes (15 ml). The organic phase was washed twice with water (15 ml), dried over Na2SO4, and concentrated in vacuum. The residue (3.7 g) was dissolved in THF (10 ml), and treated with water (7 ml) and glacial acetic acid (21 ml). After stirring for 90 minutes, the mixture was added to ice water and extracted twice with a 1:1 mixture (v/v) of diethyl ether and hexanes (30 ml). The organic phase was washed with water (30 ml), dried over Na2SO4, and concentrated in vacuum. Flash column chromatography on silica using a gradient of 5-20% methanol in DCM containing 0.2% acetic acid afforded 4-tert-butyldimethylsilyloxybenzoic acid (22, 1.42 g, 5.3 mol, 53%) as a white solid. 1H NMR (400 MHz, chloroform-d1): δ (ppm) 0.24 (s, 6H), 0.99 (s, 9H), 6.89 (d, J=8.8 Hz, 2H), 8.02 (d, J=8.8 Hz, 2H); 13C NMR (100 MHz, chloroform-d1): δ (ppm)-4.22, 18.40, 25.73, 120.08, 122.39, 132.46, 132.46, 161.01, 172.23. See FIGS. 33A-B.