ChemicalBook--->CAS DataBase List--->23680-40-2

23680-40-2

23680-40-2 Structure

23680-40-2 Structure
IdentificationBack Directory
[Name]

Methyl-3-bromopropiolate
[CAS]

23680-40-2
[Synonyms]

182050
Bexarotene Impurity 21
Methyl-3-bromopropiolate
Methyl 3-bromopropynoate
Methyl 3-bromoprop-2-ynoate
2-Propynoic acid, 3-broMo-, Methyl ester
Methyl-3-bromopropiolate ISO 9001:2015 REACH
[Molecular Formula]

C4H3BrO2
[MDL Number]

MFCD22989330
[MOL File]

23680-40-2.mol
[Molecular Weight]

162.969
Chemical PropertiesBack Directory
[Boiling point ]

40-45 °C(Press: 5 Torr)
[density ]

1.723±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[Appearance]

Colorless to light yellow <20°C Solid,>20°C Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H302+H312-H315-H319-H331-H335
[Precautionary statements ]

P261-P280-P305+P351+P338-P311
Questions And AnswerBack Directory
[Application]

3-Bromopropynate methyl ester is a pharmaceutical intermediate obtained by brominating methyl propynate with NBS. Literature reports its potential use in preparing a class of compounds for cartilage repair.
Hazard InformationBack Directory
[Synthesis Reference(s)]

Synthetic Communications, 22, p. 567, 1992 DOI: 10.1080/00397919208019255
[Synthesis]

Methyl propiolate

922-67-8

Methyl-3-bromopropiolate

23680-40-2

The general procedure for the synthesis of methyl 3-bromopropiolate from methyl propiolate: methyl propiolate (60 g, 713.6 mmol) was dissolved in acetone (2 L), followed by the sequential addition of N-bromosuccinimide (147.22 g, 827.13 mmol) and silver nitrate (12.12 g, 71.37 mmol). A slight exothermic phenomenon was observed during the reaction and the reaction temperature was increased from 21°C to 32°C. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the resulting gray suspension was evaporated by vacuum to remove the solvent, pentane (100 mL) was added and filtered through Celite, and the filter cake was washed with additional pentane. The process was repeated twice and all filtrates were combined and vacuum evaporated to give 113 g of methyl 3-bromopropiolate in 98% yield, which contained about 10% unreacted material. The product was characterized by 1H NMR (400 MHz, CDCl3) with a chemical shift δ of 3.78 (s, 3H).

[References]

[1] Patent: WO2015/166373, 2015, A1. Location in patent: Page/Page column 148
[2] Organic Syntheses, 1997, vol. 74, p. 212 - 212
[3] Synthetic Communications, 1992, vol. 22, # 4, p. 567 - 572
[4] Patent: US2003/236264, 2003, A1. Location in patent: Page 44
[5] Patent: US2003/236270, 2003, A1. Location in patent: Page 33
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl-3-bromopropiolate(23680-40-2)1HNMR
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