ChemicalBook--->CAS DataBase List--->56525-42-9

56525-42-9

56525-42-9 Structure

56525-42-9 Structure
IdentificationBack Directory
[Name]

MPC
[CAS]

56525-42-9
[Synonyms]

MPC
butan-2-ylcarbonate
methyl propyl carbonate
Carbonic acid, methyl propyl ester
[Molecular Formula]

C5H10O3
[MOL File]

56525-42-9.mol
[Molecular Weight]

118.13
Chemical PropertiesBack Directory
[Boiling point ]

125 °C(Press: 630 Torr)
[density ]

0.976±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[Appearance]

Colorless to light yellow Liquid
Spectrum DetailBack Directory
[Spectrum Detail]

MPC(56525-42-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Propanol

71-23-8

Carbamic acid, (1,3-dihydro-2H-benzimidazol-2-ylidene)-, methyl ester (9CI)

162976-69-4

2-Aminobenzimidazole

934-32-7

Dipropyl carbonate

623-96-1

MPC

56525-42-9

The general procedure for the synthesis of 2-aminobenzimidazole, propyl carbonate and methylpropyl carbonate from n-propanol and compounds (CAS:162976-69-4) is as follows: amide-containing compounds having a (benzo)imidazole-2-yl group can be subjected to catalytic directional cleavage reactions with alcohol nucleophilic reagents in the presence of a metal catalyst. Specific embodiments are described in Scheme ES: using 10.0 mol% Zn(OAc)2-2H2O as a catalyst, 1.0 equivalent of ACDG-NH-C(O)-R3 (21d), and 30.0 equivalents of propanol (under sealed conditions) for a reaction time of 24 hr; wherein R is a 1H-benzo[d]imidazol-2-yl group, and R3 is an OMe. Reaction products The yields were determined by NMR analysis using TMB as an internal standard: 0% for unreacted 21d, 61% for 2-aminobenzimidazole (20d), 40% for methylpropyl carbonate (14c) and 22% for dipropyl carbonate (14d).

[References]

[1] Patent: WO2017/46133, 2017, A1. Location in patent: Page/Page column 58; 59
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