ChemicalBook--->CAS DataBase List--->33577-99-0

33577-99-0

33577-99-0 Structure

33577-99-0 Structure
IdentificationBack Directory
[Name]

methyl 2-ethynylbenzoate
[CAS]

33577-99-0
[Synonyms]

NSC 649436
methyl 2-ethynylbenzoate
Methyl o-ethynylbenzoate
Methyl 2-ethynylbenzoate 95%
o-Methoxycarbonylphenylacetylene
2-Ethynyl-benzoic acid Methyl ester
OrthoMethoxycarbonylphenylacetylene
Benzoic acid, 2-ethynyl-, methyl ester
[Molecular Formula]

C10H8O2
[MDL Number]

MFCD12547057
[MOL File]

33577-99-0.mol
[Molecular Weight]

160.17
Chemical PropertiesBack Directory
[Boiling point ]

80-85 °C(Press: 1 Torr)
[density ]

1.11±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Colorless to light yellow Solid-liquid mixture
Safety DataBack Directory
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 2-ethynylbenzoate(33577-99-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

methyl 2-((trimethylsilyl)ethynyl)benzoate

107793-07-7

methyl 2-ethynylbenzoate

33577-99-0

General procedure for the synthesis of methyl 2-[(trimethylsilyl)ethynyl]benzoate from methyl 2-alkynylbenzoate: 1. Preparation of reaction system: Cesium fluoride (1.41 g, 9.30 mmol) was added to an acetonitrile/water (20 mL/5 mL) solution of methyl 2-[(trimethylsilyl)ethynyl]benzoate (540 mg, 2.32 mmol). 2. Reaction conditions: the reaction mixture was stirred at room temperature for 4 hours. 3. Post-treatment: After completion of the reaction, the reaction mixture was concentrated and the residue was partitioned with ethyl acetate (100 mL) and 0.2 N hydrochloric acid (30 mL). The aqueous layer was extracted with ethyl acetate (100 mL), the combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated. 4. Purification: The residue was purified by column chromatography using 0 to 5% ethyl acetate/hexane as eluent to afford methyl 2-alkynylbenzoate (358 mg, 96% yield). 5. Characterization: GC/MS analysis showed a molecular ion peak m/z of 160.

[References]

[1] Tetrahedron Letters, 2003, vol. 44, # 46, p. 8525 - 8527
[2] Tetrahedron, 2007, vol. 63, # 40, p. 9979 - 9990
[3] Patent: WO2007/140174, 2007, A2. Location in patent: Page/Page column 32
[4] Organic Letters, 2010, vol. 12, # 16, p. 3651 - 3653
[5] Tetrahedron Letters, 2010, vol. 51, # 15, p. 2007 - 2009
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