Hydrochloric Acid → Oxane-4-carboxylic acid

In a flask made of glass equipped with a stirring device, a thermometer and a reflux condenser and having an inner volume of 50 ml were charged 1.0 g (5.74 mmol) of tetrahydropyran-4,4-dicarboxylic acid with purity of 100%, 21 mg (0.14 mmol) of copper(I) oxide and 3.0 ml of pyridine under nitrogen atmosphere, and the mixture was reacted at 110 to 120° C. for 1 hour under stirring. After completion of the reaction, the reaction mixture was cooled to room temperature, 5 ml of water, 5 ml (60 mmol) of conc. hydrochloric acid and 10 ml of ethyl acetate were successively added in this order to the reaction mixture. The aqueous layer and the organic layer (the ethyl acetate layer) were separated, the aqueous layer was extracted three times with each 10 ml of ethyl acetate, then, the organic layer and the ethyl acetate extracts were combined and the mixture was concentrated under reduced pressure to give 534 mg (Isolation yield: 72%) of tetrahydropyran-4-carboxylic acid with purity of 100% (analytical value by differential refractometry) as white crystals.

1. customIn a flask made of glass
2. customequipped with a stirring device
3. customthe mixture was reacted at 110 to 120° C. for 1 hour
4. customAfter completion of the reaction
5. customThe aqueous layer and the organic layer (the ethyl acetate layer) were separated
6. extractionthe aqueous layer was extracted three times with each 10 ml of ethyl acetate
7. concentrationthe mixture was concentrated under reduced pressure

ORD 기록

ord-818b5bbaffff467a925f179d93ef4326

출처 데이터셋

uspto-grants-2007_11

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07300953B2