Identification | Back Directory | [Name]
tert-butyl benzo[b]thiophen-2-ylcarbaMate | [CAS]
89673-36-9 | [Synonyms]
tert-butyl benzo[b]thiophen-2-ylcarbaMate tert-Butyl N-(1-benzothiophen-2-yl)carbamate Benzothiophene-2-carbamic acid tert-butyl ester Benzo[b]thien-2-yl-carbamic acid tert-butyl ester | [Molecular Formula]
C13H15NO2S | [MDL Number]
MFCD22056377 | [MOL File]
89673-36-9.mol | [Molecular Weight]
249.33 |
Chemical Properties | Back Directory | [Melting point ]
100-101 °C(Solv: ethanol (64-17-5)) | [Boiling point ]
333.4±15.0 °C(Predicted) | [density ]
1.234 | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [pka]
13.52±0.43(Predicted) | [Appearance]
Off-white to light yellow Solid |
Hazard Information | Back Directory | [Synthesis]
Benzo[b]thiophene-2-carboxylic acid (1-A, 14.4 g, 80.6 mmol) was used as starting material and mixed with N,N-diisopropylethylamine (15.5 mL, 88.6 mmol) and diphenylphosphoryl azide (20.8 mL, 96.7 mmol) in tert-butanol (150 mL). The reaction mixture was heated to reflux for 8 hours. Upon completion of the reaction, the solvent was removed by vacuum evaporation. The resulting residue was purified by silica gel fast column chromatography using dichloromethane as eluent to afford the target product tert-butyl benzo[b]thiophene-2-yl-carbamate (1-B) as a colorless solid (18.9 g, 94% yield). The structure of the product was confirmed by 1H-NMR (DMSO-d6) and mass spectrometry (MS): 1H-NMR (DMSO-d6) δ 1.50 (s, 9H), 6.78 (s, 1H), 7.16 (d, J=7.5Hz, 1H), 7.27 (d, J=7.5Hz, 1H), 7.58 (d, J=7.5Hz, 1H), 7.77 ( d, J=7.5Hz, 1H), 10.70 (br s, 1H); MS: m/z 250.2 (MH+). | [References]
[1] Patent: WO2009/12430, 2009, A1. Location in patent: Page/Page column 180-181 [2] Patent: US2010/160289, 2010, A1. Location in patent: Page/Page column 24-25 [3] Patent: US2012/190674, 2012, A1. Location in patent: Page/Page column 73 [4] Patent: US2007/105864, 2007, A1. Location in patent: Page/Page column 193 [5] Patent: US2007/117804, 2007, A1. Location in patent: Page/Page column 125 |
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