Sulfuric Acid → HCID 13277552, 화합물

온도

25 °C

trans i.e. (3S,4S)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinone (0.08 g) is dissolved in a mixture of tetrahydrofuran (10 ml) and water (2 ml), and 0.02 g of mercury sulfate and a catalytic amount of concentrated sulfuric acid are added, followed by stirring at 25° C. for 3 hours. After addition of 0.1 g of sodium hydrogen carbonate, the mixture is concentrated to dryness under reduced pressure. The residue is extracted with 50 ml of ethyl acetate and the extract is concentrated to dryness. The residue is dissolved in 10 ml of ethyl acetate, and m-chloroperbenzoic acid (0.2 g) is added, followed by strirring for 50 hours. After addition of 0.2 ml of dimethyl sulfide, and the mixture is stirred further for 30 minutes and concentrated under reduced pressure. The residue is subjected to silica gel column chromatography (eluent: 60% ethyl acetate-40% n-hexane) to give trans i.e. (3S,4R)-4-acetoxy-3-[(R)-1-hydroxyethyl]-2-azetidinone (0.04 g).

1. concentrationthe mixture is concentrated to dryness under reduced pressure
2. extractionThe residue is extracted with 50 ml of ethyl acetate
3. concentrationthe extract is concentrated to dryness
4. dissolutionThe residue is dissolved in 10 ml of ethyl acetate
5. additionm-chloroperbenzoic acid (0.2 g) is added
6. waitby strirring for 50 hours
7. additionAfter addition of 0.2 ml of dimethyl sulfide
8. stirringthe mixture is stirred further for 30 minutes
9. concentrationconcentrated under reduced pressure

ORD 기록

ord-14d9b31fc918400fa4ea5c428c04bca9

출처 데이터셋

uspto-grants-1989_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US04845210