Benzyl Alcohol → (1R,2S)-2-(phenylmethoxycarbonylamino)cyclohexane-1-carboxylic acid

Temperature

30 °C

A solution was prepared by dissolving 18.6 g. of cis-(±)-perhydrophthalic acid, 2,4-cyclolactone in 235 ml. of THF. 12.1 g. of triethyl amine were added thereto. Next, a solution of 31.6 g. of diphenylphosphoryl azide in 50 ml. of THF was added in dropwise fashion at room temperature. The reaction mixture was warmed at about 30° C. for 20 min. and then at reflux temperature for about 3 hrs. The reaction mixture was then cooled to room temperature and stirred at that temperature overnight. 12.4 ml. of benzyl alcohol were added. This reaction mixture was heated to reflux for three hours and was then poured into water. The aqueous mixture was extracted with methylene dichloride. (The pH of the aqueous layer was about 7). The organic extract was dried, and the volatile constituents removed to leave a colorless oil weighing 50.6 g. The residual oil was dissolved in ether, and the ethereal solution chromatographed over silica. Initial fractions were shown to be unreacted benzyl alcohol. The next material to be eluted was cis-(±)-2-benzyloxycarbonylaminocyclohexanecarboxylic acid, 1,3-cyclolactone. 9.5 g. of a white solid product were obtained.

1. customA solution was prepared
2. dissolutionby dissolving 18.6 g
3. temperatureat reflux temperature for about 3 hrs
4. temperatureThe reaction mixture was then cooled to room temperature
5. temperatureThis reaction mixture was heated
6. temperatureto reflux for three hours
7. extractionThe aqueous mixture was extracted with methylene dichloride
8. extractionThe organic extract
9. customwas dried
10. customthe volatile constituents removed
11. customto leave a colorless oil
12. customthe ethereal solution chromatographed over silica
13. washThe next material to be eluted
14. customof a white solid product were obtained

ORD record

ord-143fbc3506ed426cbc3b71bb71d4f65f

Source dataset

uspto-grants-1985_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04537964