Basic information Safety Supplier Related

2,3-DIHYDRO-4-BENZOFURANAMINE

Basic information Safety Supplier Related

2,3-DIHYDRO-4-BENZOFURANAMINE Basic information

Product Name:
2,3-DIHYDRO-4-BENZOFURANAMINE
Synonyms:
  • 2,3-DIHYDRO-4-BENZOFURANAMINE
  • 2,3-dihyro-4-benzofuranamine
  • 2,3-dihydrobenzofuran-4-aMine
  • 5H,6H,7H,7aH-cyclopenta[b]pyran-5-aMine
  • 2,3-Dihydro-1-benzofuran-4-amine
  • 2,3-Dihydro-1-benzofuran-4-ylamine
  • 2,3-dihydrobenzofuran-4-amine hydrochloride
  • 4-Amino-2,3-dihydrobenzofuran
CAS:
61090-37-7
MF:
C8H9NO
MW:
135.16
Mol File:
61090-37-7.mol
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2,3-DIHYDRO-4-BENZOFURANAMINE Chemical Properties

Boiling point:
268.5±29.0 °C(Predicted)
Density 
1.208±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
3.94±0.20(Predicted)
Appearance
Off-white to light brown Solid
InChI
InChI=1S/C8H9NO/c9-7-2-1-3-8-6(7)4-5-10-8/h1-3H,4-5,9H2
InChIKey
RWPLKRGISDOAAG-UHFFFAOYSA-N
SMILES
O1C2=CC=CC(N)=C2CC1
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Safety Information

HS Code 
2932990090
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2,3-DIHYDRO-4-BENZOFURANAMINE Usage And Synthesis

Synthesis

76093-72-6

61090-37-7

Synthesis of 4-amino-2,3-dihydrobenzofuran (1c): compound 1b (4.10 g, 16.3 mmol) was dissolved in 48% aqueous hydrobromic acid solution (20.0 mL) and mixed with thorough stirring. The reaction mixture was heated to reflux at 110°C for 16 hours. Upon completion of the reaction, the mixture was cooled to room temperature, followed by the slow addition of sodium hydroxide pellets in an ice bath at 0°C to adjust the pH to about 9. The reaction mixture was extracted several times with ethyl acetate (50 mL × 4). The organic phases were combined, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give the crude product. Purification of the crude product by medium pressure column chromatography (Smart Flash EPCLC W-Prep 2XY system, eluent: hexane/ethyl acetate = 1/1) afforded 4-amino-2,3-dihydrobenzofuran (Compound 1c) (1.49 g, 11.0 mmol, 67.7% yield) as a colorless solid. tlc Rf = 0.30 (unfolding agent: Hexane/ethyl acetate = 1/1).1H NMR (400 MHz, CDCl3) δ 6.94 (dd, J = 8.4, 8.4 Hz, 1H), 6.28 (dd, J = 0.4, 7.6 Hz, 1H), 6.23 (dd, J = 0.4, 7.6 Hz, 1H), 4.59 (t, J = 8.4 Hz, 2H), 3.60 ( br s, 2H), 3.02 (t, J = 8.4 Hz, 2H).

References

[1] Patent: EP2881397, 2015, A1. Location in patent: Paragraph 0053; 0058; 0059
[2] Patent: US2016/303089, 2016, A1. Location in patent: Paragraph 0161; 0168; 0169; 0170; 0171
[3] Patent: US2008/318941, 2008, A1. Location in patent: Page/Page column 39
[4] Patent: WO2009/23844, 2009, A2. Location in patent: Page/Page column 127-128
[5] Patent: US2008/200471, 2008, A1. Location in patent: Page/Page column 60; 61-62

2,3-DIHYDRO-4-BENZOFURANAMINESupplier

Shanghai Birch Chemical Technology Co., Ltd. Gold
Tel
021-54096810 18017263450
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sales@birchchem.com
Energy Chemical
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021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
18270980682
Email
mlcheng@sunwaypharm.cn
Atop-Pharma (Shanghai) Technology Co., Ltd.
Tel
+86 (21) 5196-9732
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Email
product02@bidepharm.com
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