ChemicalBook--->CAS DataBase List--->21857-45-4

21857-45-4

21857-45-4 Structure

21857-45-4 Structure
IdentificationMore
[Name]

5-Methoxy-2,3-dihydroindoline
[CAS]

21857-45-4
[Synonyms]

1H-INDOLE, 2,3-DIHYDRO-5-METHOXY-
5-METHOXY-2,3-DIHYDRO-1H-INDOLE
5-METHOXY-2,3-DIHYDROINDOLINE
5-METHOXYLINDOLINE
5-Methoxyindoline
5-Methoxy-2,3-dihydro-1H-indoline
[Molecular Formula]

C9H11NO
[MDL Number]

MFCD07368037
[Molecular Weight]

149.19
[MOL File]

21857-45-4.mol
Chemical PropertiesBack Directory
[Boiling point ]

282.6±29.0 °C(Predicted)
[density ]

1.076±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

6.07±0.20(Predicted)
[Appearance]

Light yellow to brown Liquid
[InChI]

1S/C9H11NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-3,6,10H,4-5H2,1H3
[InChIKey]

YYDYAQAVAHKFJO-UHFFFAOYSA-N
[SMILES]

COc1ccc2NCCc2c1
[CAS DataBase Reference]

21857-45-4(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[WGK Germany ]

WGK 3
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

5-Methoxy-2,3-dihydroindoline(21857-45-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Methoxyindole

1006-94-6

5-Methoxy-2,3-dihydroindoline

21857-45-4

5-Methoxyindole (1.5 g, 10.2 mmol) was dissolved in acetic acid (20 mL) at 25 °C, followed by the addition of sodium cyanoborohydride (0.77 g, 12.2 mmol) in batches. After the reaction lasted for 1 h, the pH of the reaction solution was adjusted to 9-10 with 20% sodium hydroxide solution for neutralization. The reaction mixture was extracted with ethyl acetate (50 mL) and the organic phase was separated and dried over anhydrous sodium sulfate. The dried organic phase was filtered and the filtrate was concentrated by rotary evaporation. Finally, 5-methoxyindoline was purified by column chromatography (eluent: petroleum ether/ethyl acetate, 10:1, v/v) to afford 5-methoxyindoline as a brown solid (1.46 g, 95.9% yield).

[References]

[1] Organic Letters, 2011, vol. 13, # 19, p. 5124 - 5127
[2] Chemical Communications, 2013, vol. 49, # 63, p. 7052 - 7054
[3] Patent: CN105367474, 2016, A. Location in patent: Paragraph 0194; 0195; 0196; 0197
[4] Journal of Medicinal Chemistry, 1997, vol. 40, # 4, p. 479 - 485
[5] Patent: EP1223170, 2002, A1
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