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Chemical Structure| 309741-11-5 Chemical Structure| 309741-11-5

Structure of 309741-11-5

Chemical Structure| 309741-11-5

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Product Details of [ 309741-11-5 ]

CAS No. :309741-11-5
Formula : C12H12BrNO
M.W : 266.13
SMILES Code : OC1C(NC2=C3C=C(Br)C=C2)=C3CCC1

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Application In Synthesis of [ 309741-11-5 ]

* 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 [ 309741-11-5 ]

[ 309741-11-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 59514-18-0 ]
  • [ 309741-11-5 ]
YieldReaction ConditionsOperation in experiment
50% With sodium borohydrid; In methanol; ethyl acetate; a) 6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-ol To a solution of <strong>[59514-18-0]6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one</strong> (500 mg, 1.9 mmol) in methanol (20 mL) was added sodium borohydride (144 mg, 3.8 mmol) portionwise. The reaction mixture was stirred for one hour and quenched with water (5 mL). The reaction was concentrated, diluted with methylene chloride and washed with water. The organic phase was concentrated and the crude alcohol purified by flash chromatography on silica (5% to 30% ethyl acetate/hexanes gradient) to provide 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-ol (255 mg, 50%) as a light brown solid: 1H-NMR (DMSO-d6): delta 10.99 (s, 1H), 7.54 (d, 1H), 7.25 (d, 1H), 7.12 (dd, 1H), 5.18 (d, 1H), 4.75-4.70 (m, 1H), 2.64-2.53 (m, 2H), 2.02-1.91 (m, 2H), 1.77-1.66 (m, 2H); MS m/z (M-1) 339, 341.
50% With sodium tetrahydroborate; In methanol; for 1h; Example 33: 6-BROMO-N- (1-METHVL-1-PHENVLETHVL)-2, 3, 4, 9-TETRAHVDRO-1H-CARBAZOL-1- amine hydrochloride salt To a solution of 6-bromo-2,3, 4, 9-tetrahydro-1H-carbazol-1-one (500 mg, 1.9 MMOL) in methanol (20 mL) was added sodium borohydride (144 mg, 3.8 MMOL) portionwise. The reaction mixture was stirred for one hour and quenched with water (5 mL). The reaction was concentrated, diluted with methylene chloride, and washed with water. The organic phase was concentrated and the crude alcohol purified by flash chromatography on silica (5% to 30% ethyl acetate/hexanes gradient) to provide 6- bromo-2,3, 4, 9-TETRAHYDRO-1H-CARBAZOL-1-OL (255 mg, 50%). as a light brown solid.'H- NMR (DMSO-DE) : 8 10.99 (s, 1H), 7.54 (d, 1H), 7.25 (d, 1H), 7.12 (dd, 1H), 5.18 (d, 1 H), 4.75-4. 70 (m, 1H), 2.64-2. 53 (m, 2H), 2.02-1. 91 (m, 2H), 1.77-1. 66 (m, 2H); MS m/z (M+1) 267. 6-bromo-N-(1-methyl-1-phenylethyl)-2, 3,4, 9-tetrahydro-1 H-carbazol-1-amine hydrochloride salt was prepared by dissolving 6-bromo-2,3, 4, 9-TETRAHYDRO-1H- carbazol-1-ol (0.04 g, 0.15 MMOL) in cumyl amine (0.5 mL) in the presence of p- toluene sulfonic acid in a 2 mL reaction vessel with a stir bar. The vessel was sealed and heated in a Personal Chemistry Microwave Synthesizer for 10 min. at 150C. The crude reaction was purified by flash chromatography on silica (5% to 25% ethyl acetate/hexanes gradient) and converted to the HCI salt to afford a white solid (14 MG, 22%). 1H-NMR (DMSO-d6) : No. 11.20 (s, 1 H), 9.50 (s, 1 H), 9.06 (s, 1 H), 7.79 (d, J=7.0 Hz, 2H), 7.64 (d, J=1.8 Hz, 1 H), 7.49 (t, J=7.0 Hz, 2H), 7.43 (t, J=7.0 Hz, 1 H), 7.37 (d, J=8.6 Hz, 2H), 7.24 (dd, J=8.6 Hz, J=1. 8 Hz, 1H), 4.47 (s, 1 H), 2.67-2. 60 (m, 1 H), 2.47-2. 20 (m, 1 H), 2.00 (s, 3H), 1.81 (m, 4H) 1.59-1. 34 (m, 3H); MS M/Z 381, 383 (M-1); Anal. Calcd. For C2IHZ4BRN2C . : C, 60.08 ; H, 5.76 ; N, 6.67. Found: C, 60.01 ; H, 5.84 ; N, 6.67.
 

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