Sodium Chloride → 4-Tetrahydropyranyloxy-2-(6-tetrahydropyranylcarboxyhexyl)cyclopent-2-en-1-one

HRID 461259Notes

Reaction equation

HRID 461259 reaction equation
[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[C:11](=[O:16])[CH2:12][CH:13]([OH:15])[CH:14]=1)([OH:3])=[O:2].[O:17]1[CH:22]=[CH:21][CH2:20][CH2:19][CH2:18]1.O.[C:24]1(C)C=[CH:28][C:27](S(O)(=O)=O)=[CH:26][CH:25]=1.C(=O)(O)[O-:36].[Na+].[Cl-].[Na+]>O.CCOCC.C(Cl)Cl>[O:17]1[CH2:18][CH2:19][CH2:20][CH2:21][CH:22]1[O:15][CH:13]1[CH2:12][C:11](=[O:16])[C:10]([CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH:4]([C:1]([OH:3])=[O:2])[CH:28]2[CH2:27][CH2:26][CH2:25][CH2:24][O:36]2)=[CH:14]1

Participants

9

Reactant 5

HCID 5234Sodium ChlorideHCID 80803,4-dihydro-2H-pyranHCID 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrateHCID 3690897ACMC-20apjz

Product 1

HCID 704200994-Tetrahydropyranyloxy-2-(6-tetrahydropyranylcarboxyhexyl)cyclopent-2-en-1-one

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 3283Diethyl EtherSolventHCID 6344DichloromethaneSolvent

Procedure

To a stirred solution of 5.59 g. (24.6 mmoles) of 4-hydroxy-2-(6-carboxyhexyl) cylopent-2-en-1-one (Example 122) and 20.7 g. (2.46 mmoles) of dihydropyran in 100 ml. of methylene chloride at 20° C. is added 47 mg. (0.246 mmoles) of p-toluenesulfonic acid monohydrate in one portion. The temperature is maintained at 20°-25° C. by cooling and is stirred for one hour at that temperature. The solution is diluted with 200 ml. of ether and poured into a mixture of 40 ml. of saturated sodium bicarbonate solution, 40 ml. of saturated sodium chloride solution, and 80 ml. of water. The phases are separated, and the aqueous phase is extracted with additional ether. The total extract is washed successively with water and saturated sodium chloride solution, dried over potassium carbonate, and freed of volatile matter by concentration at reduced pressure to give an oil, λ maxMeOH. = 223 mu (9500); ν max. 1730 (ester carbonyl group), 1705 (ketone carbonyl group), and 1030 cm-1 (tetrahydropyranyloxy groups).

Workup

  1. temperatureThe temperature is maintained at 20°-25° C.
  2. temperatureby cooling
  3. additionThe solution is diluted with 200 ml
  4. customThe phases are separated
  5. extractionthe aqueous phase is extracted with additional ether
  6. extractionThe total extract
  7. washis washed successively with water and saturated sodium chloride solution
  8. dry with materialdried over potassium carbonate
  9. concentrationfreed of volatile matter by concentration at reduced pressure
  10. customto give an oil, λ maxMeOH

Sources & evidence

ORD record
ord-320fb0d7b0a94710b57f169ce8dba66d
Source dataset
uspto-grants-1977_12
Patent number
US04061672

Reaction notes

Loading…