반응 #43515

반응 방정식

hydrochloric acid

1-tert-butoxycarbonyl-4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine-4-ol

di-tert-butyl dicarbonate

sodium hydroxide

→

4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester

수율 48.2%

용매

acetic acid

triethyl amine

반응 조건

후처리

1. 1
   온도The solution was refluxed overnight
2. 2
   추출the unclear solution was extracted with ethyl acetate (3×450 mL)
3. 3
   세척The combined organic phases were washed with saturated aqueous sodium chloride (450 mL)
4. 4
   건조dried over magnesium sulfate
5. 5
   기타the solvents evaporated off
6. 6
   workup.DISSOLUTIONThe crude material (8.02 g) was dissolved in THF (195 mL)
7. 7
   workup.STIRRINGThe mixture was stirred overnight
8. 8
   기타quenched by addition of saturated aqueous ammonium chloride (200 mL)
9. 9
   건조The organic phase was dried over magnesium sulfate
10. 10
    기타the solvent was evaporated off
11. 11
    기타The crude material was purified by chromatography on silica gel (eluent

실험 절차

Concentrated aqueous hydrochloric acid (150 mL) was added to a stirred solution of 1-tert-butoxycarbonyl-4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine-4-ol (12.13 g, 28.9 mmol) in acetic acid (450 mL). The solution was refluxed overnight, cooled to room temperature and then stirred on an ice bath. A saturated aqueous solution of sodium hydroxide (250 mL) was slowly added and the unclear solution was extracted with ethyl acetate (3×450 mL). The combined organic phases were washed with saturated aqueous sodium chloride (450 mL), dried over magnesium sulfate and the solvents evaporated off. The crude material (8.02 g) was dissolved in THF (195 mL) and di-tert-butyl dicarbonate (Boc2O, 6.96 g, 31.9 mmol) and triethyl amine (5 mL) were added. The mixture was stirred overnight and then quenched by addition of saturated aqueous ammonium chloride (200 mL). The organic phase was dried over magnesium sulfate, and the solvent was evaporated off. The crude material was purified by chromatography on silica gel (eluent: An increasing amount of ethyl acetate (0-20%) in heptane) to produce 4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester as a white solid (5.63 g). This material was dissolved in methylene chloride (130 mL). Hydrogen gas (3 bar) was bubbled through the solution using a Parr shaker apparatus and (1,5-cyclooctadiene)(pyridine)(tricyclohexylphosphine)(hexafluorophosphine) iridium(I) (Crabtree's catalyst, 0.495 g, 1.40 mmol) was added and the hydrogenation was allowed to continue overnight. The catalyst was filtered off and the crude product was purified by chromatography on silica gel (eluent: An increasing amount of ethyl acetate (0-20%) in heptane) to produce 4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester (5.37 g). This material was dissolved in methanol (70 mL) and hydrogen chloride in diethyl ether (2M, 67 mL, 133 mmol) was added and the reaction mixture was stirred overnight. The solvent was evaporated off, and aqueous sodium hydroxide (2M, 200 mL), and ethyl acetate (400 mL) were added. The phases were separated, and the aqueous phase was extracted with ethyl acetate (400 mL). The combined organic phases were washed with saturated aqueous sodium chloride (300 mL), dried over magnesium sulfate, and the solvent was evaporated off. The residue was purified by chromatography on silica gel (eluent: An increasing amount of ethanol (0-25%) in ethyl acetate containing 5% triethyl-amine) to produce 4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine (1.63 g). This material was dissolved in THF at 50° C. and a solution of oxalic acid (0.48 g) in THF was slowly added. 4-[2-(4-chloro-phenylsulfanyl)-phenyl]-piperidine oxalic acid salt was collected as a white solid. LC/MS (m/z) 304.0 (MH+); RT=2.29; purity (UV, ELSD): 96%, 96%; yield: 1.86 g (15%).

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