Triethylamine → 3alpha, 7beta-Ditetrahydropyranyloxy-5beta-cholan-24-al

HRID 2371862Notes

Reaction equation

HRID 2371862 reaction equation
C(Cl)(=O)C(Cl)=O.[O:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[O:13][C@@H:14]1[CH2:36][CH2:35][C@@:34]2([CH3:37])[C@H:16]([CH2:17][C@H:18]([O:39][CH:40]3[CH2:45][CH2:44][CH2:43][CH2:42][O:41]3)[C@@H:19]3[C@@H:33]2[CH2:32][CH2:31][C@@:30]2([CH3:38])[C@H:20]3[CH2:21][CH2:22][C@@H:23]2[C@H:24]([CH3:29])[CH2:25][CH2:26][CH2:27][OH:28])[CH2:15]1.C(N(CC)CC)C>C(Cl)Cl.CS(C)=O.O>[O:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[O:13][C@@H:14]1[CH2:36][CH2:35][C@@:34]2([CH3:37])[C@H:16]([CH2:17][C@H:18]([O:39][CH:40]3[CH2:45][CH2:44][CH2:43][CH2:42][O:41]3)[C@@H:19]3[C@@H:33]2[CH2:32][CH2:31][C@@:30]2([CH3:38])[C@H:20]3[CH2:21][CH2:22][C@@H:23]2[C@H:24]([CH3:29])[CH2:25][CH2:26][CH:27]=[O:28])[CH2:15]1

Participants

7

Reactant 3

HCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 228428353alpha,7beta-Ditetrahydropyranyloxy-5beta-cholan-24-ol

Product 1

HCID 867455493alpha, 7beta-Ditetrahydropyranyloxy-5beta-cholan-24-alYield 86.8%

Reagents, catalysts & solvents 3

HCID 679Dimethyl SulfoxideSolvent2×HCID 962WaterSolventHCID 6344DichloromethaneSolvent3×

Procedure

To a solution of oxalyl chloride (8.17 g; 64.35 mmoles) in methylene chloride (140 ml) kept at -70° C. under magnetic stirring and nitrogen atmosphere, dimethylsulfoxide (11.00 g; 141.15 mmoles) diluted in methylene chloride (10 ml) was added in about 10 min. The reaction mixture was left to stand for 10 min., then a solution of compound (3) (29.60 g; 54.15 mmoles) in methylene chloride (20 ml) and dimethylsulfoxide (20 ml) was dropped therein in about 20 min. 15 Min. after, triethylamine (29.73 g; 294.4 mmoles) was added and the resulting mixture was kept under stirring for 10 min. The reaction mixture was warmed to r.t., diluted with water (200 ml), the organic phase was separated and the aqueous one was extracted with methylene chloride (3×50 ml). The combined organic phases were washed with saturated water (1×50 ml), dried over sodium sulfate and concentrated under vacuum. The residue (31.50 g) was subjected to flash chromatography on SiO2 (φ 5.5 cm, h=25 cm): eluting with 4/6 ethyl ether/petroleum ether, 25.6 g of compound (4) were obtained, (87%); max (CHCl3): 1725 cm-1 (C=O); 1H-NMR (CDCl3)δ 0,7 (s, 3H, 18-CH3); 0,9-0,95 (m, 6H, 19-CH3, 21-CH3); 3,1-4,1 (m, 6H, 3-CH-, 7-CH- e 2x-OCH2 -); 4,35-4,7 (m, 2H, 2x-O-CH-O-); 9,6 (s, 1H, --CHO).

Workup

  1. customkept at -70° C.
  2. additionwas added in about 10 min
  3. waitThe reaction mixture was left
  4. waitin about 20 min
  5. stirringunder stirring for 10 min
  6. customthe organic phase was separated
  7. extractionthe aqueous one was extracted with methylene chloride (3×50 ml)
  8. washThe combined organic phases were washed with saturated water (1×50 ml)
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated under vacuum
  11. washeluting with 4/6 ethyl ether/petroleum ether

Sources & evidence

ORD record
ord-ac3ea897281249259e4a8a5da4cb3c94
Source dataset
uspto-grants-1992_03
Patent number
US05096898

Reaction notes

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