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Chemical Structure| 206347-32-2 Chemical Structure| 206347-32-2

Structure of 206347-32-2

Chemical Structure| 206347-32-2

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Product Details of [ 206347-32-2 ]

CAS No. :206347-32-2
Formula : C8H7Br3O
M.W : 358.85
SMILES Code : BrCCOC1=C(Br)C=CC=C1Br
MDL No. :MFCD11119884

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Application In Synthesis of [ 206347-32-2 ]

* 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 [ 206347-32-2 ]

[ 206347-32-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 206347-32-2 ]
  • [ 206347-30-0 ]
YieldReaction ConditionsOperation in experiment
78% With n-butyllithium; In tetrahydrofuran; hexane; at -78 - 0℃; for 1h; Synthesis of 7-Bromo-2,3-dihydro-benzofuran A solution of 2.5M n-BuLi (13.0 ml, 32.5 mmol) was added to a solution of 1,3-dibromo-2-(2-bromo-ethoxy)-benzene (11.5, 32.0 mmol) in 115 ml of THF and 28 ml of hexane at -78 C. over 30 mins. The reaction was continued at -78 C. for 30 minutes, then warmed to 0 C. The mixture was poured into water (100 ml) and the aqueous phase was extracted with ether. The combined organic layers were dried over Na2SO4, filtered, and concentrated to give a pale yellow oil. Silica gel chromatography using a gradient of ethyl acetate in hexanes to give 7-bromo-2,3-dihydro-benzofuran as colorless needles (5.00 g, 78%). 1H NMR (500 MHz, DMSO-d6) delta 7.27(dd, 1 Hz, 8 Hz, 1H), 7.20 (dd, 1 Hz, 7.5 Hz, 1H), 6.75 (t, 7.8 Hz, 1H), 4.59 (t, 9 Hz, 2H), 3.28 (t, 8.8 Hz, 2H).
With n-butyllithium; In tetrahydrofuran; hexane; at -80℃; 1-(2,3-Dihydrobenzofuran-7-yl)piperazine (C7i); In detail, for the synthesis of compound C7i 2,6-dibromophenole (29 mmol) (C8a; R4-R6 = H) is mixed with 1,2-dibromoethane (29 mmol) (r = 1) unter basic aqueous conditions (NaOH) and heated at reflux for 18 hrs. The resulting monoalkylation product can be solved in THF/hexane (4/1), cooled to -80 C and then, a solution of 2,5 M butyllithium (18mmol) in hexane is added dropwise (17.1 mmol). The cyclisation product 7-bromo-2,3-dihydrobenzofurane (4 mmol) (C8b; r = 1) can be suspended together with NaOtBu (20 mmol), Pd2(dba)3 (2 mol%), BINAP (2 mol%) and piperazine (8 mmol) in 5 ml dry toluene and heated at 117C for 6 hrs to get the product.
With n-butyllithium; In tetrahydrofuran; at -100℃; 2. Synthesis of 2,3-dihydrobenzofuran-7-sulfonyl chloride; n-Butyllithium (23 mmol) was added dropwise to a solution of 1,3-dibromo-2-(2-bromoethoxy)benzene (21.8 mmol) in tetrahydrofuran (100 mL) at -100 C. and the reaction mixture was maintained for 30 min. n-Butyllithium (23 mmol) was added dropwise and the reaction mixture was maintained at -100 C. for an additional 60 min. Sulfur dioxide (43.8 mmol) was added and the reaction mixture was maintained for 2 h between -100 and -85 C. The reaction mixture was diluted with hexane (100 mL) and the precipitated solids were collected by filtration. The solid was suspended in dichloromethane (100 mL) at 0 C. and N-chlorosuccinamide (24.6 mmol) was added in several batches. The reaction mixture was maintained for 60 min at 0 C. and was diluted with dichloromethane (100 mL). The reaction mixture was washed with (2 M) sodium hydrogen sulfate (2×150 mL) and brine (3×100 mL), was dried (sodium sulfate), and was concentrated. The residue was purified by Flash chromatography (1/50 ethyl acetate/petroleum ether) to provide 2,3-dihydrobenzofuran-7-sulfonyl chloride in 51% yield as a light yellow solid. Data: 1H NMR: (CDCl3) delta 3.35 (t, 2H), 4.92 (t, 2H), 6.96 (t, 1H), 7.54 (s, 1H), 7.64 (d, 1H). LC/MS (ES) m/z 283 [C13H18N2O3S+H]+.
  • 2
  • [ 206347-32-2 ]
  • [ 496-16-2 ]
  • [ 206347-30-0 ]
YieldReaction ConditionsOperation in experiment
With n-butyllithium; In tetrahydrofuran; hexane; at -78 - 0℃;Cooling with ethanol-dry ice; INTERMEDIATE 77 7-Bromo-2, 3-dihydrobenzofuran* A solution of 2- (2, 6-dibromphenoxy) ethyl bromide (1.08 g, 3 mmol; Intermediate 76) in a mixture of THF (12 mL) and hexane (3 mL) was cooled in a ethanol/dry ice bath for 30 min. n-BuLi in hexane (2 mL of 1.5 M solution) was added dropwise over 15 min. The reaction mixture was stirred at-78 C for another 30 min after which time the bath was allowed to slowly warm to 0 C. The mixture was poured onto water and extracted with diethyl ether (2x100 mL). The combined extract was dried and concentrated to give a pale brown oil (0.5 g) containing the product contaminated with approximately 25 % 2,3- dihydrobenzofuran. This material was used as such for further synthesis but could if necessary be purified by flash chromatography [eluent : hexane- EtOAc/hexane (5: 95) ]. 'H NMR (400 MHz, CDC13) 8 3.30 (t, 2 H), 4.65 (t, 2 H), 6.71 (t, 1 H), 7.11 (dd, 1 H), 7.25 (dd, 1 H). *Previously reported in Tetrahedron Lett. 1998,39, 2219-2222.
 

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