ChemicalBook--->CAS DataBase List--->1444-12-8

1444-12-8

1444-12-8 Structure

1444-12-8 Structure
IdentificationBack Directory
[Name]

Methyl 1-Methyl-1H-indole-4-carboxylate
[CAS]

1444-12-8
[Synonyms]

Methyl 1-Methylindole-4-carboxylate
Methyl 1-Methyl-4-indolecarboxylate
4-(Methoxycarbonyl)-1-methyl-1H-indole
Methyl 1-Methyl-1H-indole-4-carboxylate
1-methyl-1H-Indole-4-carboxylic acid methyl ester
1H-Indole-4-carboxylic acid, 1-methyl-, methyl ester
[Molecular Formula]

C11H11NO2
[MDL Number]

MFCD09839048
[MOL File]

1444-12-8.mol
[Molecular Weight]

189.21
Chemical PropertiesBack Directory
[Melting point ]

53 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4))
[Boiling point ]

320.2±15.0 °C(Predicted)
[density ]

1.14±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Light yellow to yellow Crystal
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P280
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 1-Methyl-1H-indole-4-carboxylate(1444-12-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl indole-4-carboxylate

39830-66-5

Iodomethane

74-88-4

Methyl 1-Methyl-1H-indole-4-carboxylate

1444-12-8

To a 40 mL reaction vial was added a solution of methyl 1H-indole-4-carboxylate (400 mg, 2.28 mmol, 1.00 equiv) in N,N-dimethylformamide (10 mL). Sodium hydride (275 mg, 6.88 mmol, 3.00 equiv, 60% dispersed in mineral oil) was added in batches at 0 °C. After keeping stirring at 0 °C for 0.5 h, iodomethane (1.298 g, 9.14 mmol, 4.00 eq.) was slowly added dropwise at the same temperature. The reaction mixture was warmed to 25 °C and stirred for 15 hours. After completion of the reaction, the mixture was poured into ice water (50 mL) and extracted with ethyl acetate (50 mL x 3). The organic phases were combined, washed with saturated saline (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated. Methyl 1-methyl-4-indolecarboxylate (429 mg, 99%) was obtained as a red oil after concentration under reduced pressure. Mass spectrum (electrospray ionization, m/z): [M+H]+ 190.

[References]

[1] Patent: WO2017/205296, 2017, A1. Location in patent: Paragraph 78
[2] Patent: US2009/298809, 2009, A1. Location in patent: Page/Page column 17
[3] Heterocycles, 2006, vol. 67, # 2, p. 643 - 653
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