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Chemical Structure| 33839-12-2 Chemical Structure| 33839-12-2

Structure of 33839-12-2

Chemical Structure| 33839-12-2

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Product Details of [ 33839-12-2 ]

CAS No. :33839-12-2
Formula : C17H19BrO
M.W : 319.24
SMILES Code : CC(C)(C)C1=CC(Br)=CC=C1OCC1=CC=CC=C1
MDL No. :MFCD31555988

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Application In Synthesis of [ 33839-12-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 33839-12-2 ]

[ 33839-12-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 10323-39-4 ]
  • [ 100-44-7 ]
  • [ 33839-12-2 ]
YieldReaction ConditionsOperation in experiment
583 mg To a solution of <strong>[10323-39-4]4-bromo-2-tert-butylphenol</strong> (CAS: 10323-39-4; 500 mg) in DMF (5 mL) was added NaH (114 mg) and the reaction mixture was stuffed for 10 minutes at rt. Then,benzylchloride (290 mg) was added and the reaction mixture was stuffed for 2 hours at rt. The mixture was poured on 30 mL 10% aqueous NH4C1 solution and 30 mL EtOAc and the layers were separated. The aqueous layer was extracted a second time with 30 mL EtOAc. The organic layers were washed with 30 mL brine, dried over Mg504, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with a gradient of n-heptane inethyl acetate (100/0 to 80/20) to give the title compound as a colorless solid (583 mg. MS (mlz):318 [Mf?.
  • 2
  • [ 10323-39-4 ]
  • [ 100-39-0 ]
  • [ 33839-12-2 ]
YieldReaction ConditionsOperation in experiment
80% With caesium carbonate; In acetonitrile; at 63℃; for 5h;Heating; Example 47B 1-B ENZYLOXY-4-BROMO-2-TERT-BUTYL-BENZENE The compound of Example 47A (2.24 g, 9.77 mmol), benzyl bromide (1.4 mL, 11.72 mmol) and cesium carbonate (4.77 g, 14.65 mmol) were mixed in 10 ML of acetonitrile. The mixture was heated to 63 C. AFTER 5 hours, the mixture was filtered and the filtrate was concentrated. The resulting residue was purified by silica gel chromatography (100% hexane) to provide the title compound (2.49 g, 80%).
80% With caesium carbonate; In acetonitrile; at 63℃; for 5h; EXAMPLE 47B 1-Benzyloxy-4-bromo-2-tert-butyl-benzene The compound of Example 47A (2.24 g, 9.77 mmol), benzyl bromide (1.4 mL, 11.72 mmol) and cesium carbonate (4.77 g, 14.65 mmol) were mixed in 10 mL of acetonitrile. The mixture was heated to 63 C. After 5 hours, the mixture was filtered and the filtrate was concentrated. The resulting residue was purified by silica gel chromatography (100% hexane) to provide the title compound (2.49 g, 80%).
11 g With caesium carbonate; In acetonitrile; at 25 - 85℃; for 3h;Inert atmosphere; This material which is known in the literature (CAS: 33839-12-2) was made as follows:To a solution of 4-bromo-2-tert-butyl-phenol (CAS: 10323-39-4; 8 g) in anhydrous acetonitrile (150 mL) was added Cs2CO3 (22.7 g) followed by benzyl bromide (6.26 mL) at 25C and the mixture was stilTed at 85C for 3h. The reaction mixture was cooled to 25C, filtered and the filtrate was evaporated under reduced pressure. The resulting residue was purified by column chromatography over silica gel (gradient of 3-5% ethyl acetate in hexanes) to provide 1-benzyloxy-4-bromo-2-tert-butyl-benzene (11.0 g) as an off white solid. ?H-NMR (400MHz, , DMSO-D6): 1.32 (s, 9H), 5.14 (s, 2H), 7.04 (d, 1H), 7.28-7.50 (m, -7H).
 

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