Hexane → HCID 57709120, compound

A 0.5 N potassium bisulfate aqueous solution (4.0 mL) was added to a suspension of dicyclohexylammonium (S)-t-butoxycarbonylamino-(4-chloro-phenyl)acetate (307 mg, 0.657 mmol) in ether (8.0 mL) at room temperature, and the mixture was stirred for 10 minutes. Then, the ether layer was separated, and the aqueous layer was extracted with ether (2×8 mL) and combined with the organic layer. The ether layer was washed with water (12 mL), dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was dissolved in benzene (1.8 mL) and methanol (0.9 mL). A solution of trimethylsilyldiazomethane in hexane (2 M, 0.36 mL, 0.72 mmol) was added dropwise under cooling with ice over five minutes, and then the mixture was stirred under cooling with ice for 10 minutes. The reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate=5/1) to give the title compound (190 mg, 96%).

1. customThen, the ether layer was separated
2. extractionthe aqueous layer was extracted with ether (2×8 mL)
3. washThe ether layer was washed with water (12 mL)
4. dry with materialdried over anhydrous magnesium sulfate
5. concentrationconcentrated under reduced pressure
6. dissolutionThe resulting residue was dissolved in benzene (1.8 mL)
7. temperatureunder cooling with ice over five minutes
8. stirringthe mixture was stirred
9. temperatureunder cooling with ice for 10 minutes
10. concentrationThe reaction mixture was concentrated under reduced pressure
11. customThe residue was purified by silica gel chromatography (hexane/ethyl acetate=5/1)

ORD record

ord-fdcae3f3ada04e2485e58aeaf2cbefc6

Source dataset

uspto-grants-2011_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07935688B2