ChemicalBook--->CAS DataBase List--->53662-85-4

53662-85-4

53662-85-4 Structure

53662-85-4 Structure
IdentificationBack Directory
[Name]

Methyl tetrahydro-3-furoate
[CAS]

53662-85-4
[Synonyms]

Methyl tetrahydro-3-furoate
Methyl tetrahydrofuran-3-...
methyl oxolane-3-carboxylate
Methyl tetrahydrofuran-3-carboxylate
3-Furancarboxylic acid, tetrahydro-, methyl ester
[Molecular Formula]

C6H10O3
[MDL Number]

MFCD06203928
[MOL File]

53662-85-4.mol
[Molecular Weight]

130.14
Chemical PropertiesBack Directory
[Boiling point ]

61-65 °C(Press: 12 Torr)
[density ]

1.108±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Flame (GHS02)
GHS07,GHS02
[Signal word ]

Warning
[Hazard statements ]

H335-H226-H302-H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2932190090
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl tetrahydro-3-furoate(53662-85-4)1HNMR
Methyl tetrahydro-3-furoate(53662-85-4)13CNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

TETRAHYDRO-3-FUROIC ACID

89364-31-8

Methyl tetrahydro-3-furoate

53662-85-4

Concentrated sulfuric acid (27.54 mL, 517 mmol) was slowly added to a solution of tetrahydro-3-furancarboxylic acid (20.00 g, 172 mmol) in methanol (350 mL). The reaction mixture was heated to reflux and kept for 18 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated in a rotary evaporator to remove most of the methanol. The concentrated residue was dissolved in water (500 mL) and dichloromethane (200 mL) for partitioning. The organic and aqueous phases were separated and the aqueous phase was extracted once more with dichloromethane (200 mL). All organic phases were combined and washed sequentially with saturated aqueous sodium bicarbonate (200 mL) and brine (200 mL). The organic phases were dried with anhydrous sodium sulfate, filtered and concentrated to afford methyl 3-tetrahydrofurancarboxylate (15.0 g, 67% yield) as a light yellow oil. The product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 3.85 (t, J = 8.4 Hz, 1H), 3.77-3.66 (m, 3H), 3.62 (s, 3H), 3.07-3.22 (m, 1H), 1.97-2.12 (m, 2H).

[References]

[1] Journal of Organic Chemistry, 1996, vol. 61, # 8, p. 2690 - 2694
[2] Patent: US2018/201610, 2018, A1. Location in patent: Paragraph 0076; 0077
[3] Advanced Synthesis and Catalysis, 2010, vol. 352, # 2-3, p. 463 - 477
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