Sulfuric Acid → HCID 131710140, compound

HRID 1605818Notes

Reaction equation

HRID 1605818 reaction equation
[C:1]1(=[O:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:8][C@H:9]1[O:14][C@@H:13]([O:15][C@@H:16]2[CH2:32][C@:31]3([OH:33])[C@@:19]([CH:42]=[O:43])([C@@H:20]4[C@@H:28]([CH2:29][CH2:30]3)[C@:27]3([OH:34])[C@@:23]([CH3:41])([C@@H:24]([C:35]5[CH2:40][O:39][C:37](=[O:38])[CH:36]=5)[CH2:25][CH2:26]3)[CH2:22][CH2:21]4)[CH2:18][CH2:17]2)[CH2:12][C@H:11]([OH:44])[C@@H:10]1[OH:45].[BH4-].[Na+].S(=O)(=O)(O)O>O1CCOCC1>[C:1]1(=[O:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:8][CH:9]1[O:14][CH:13]([O:15][CH:16]2[CH2:32][C:31]3([OH:33])[C:19]([CH2:42][OH:43])([CH:20]4[CH:28]([CH2:29][CH2:30]3)[C:27]3([OH:34])[C:23]([CH3:41])([CH:24]([C:35]5[CH2:40][O:39][C:37](=[O:38])[CH:36]=5)[CH2:25][CH2:26]3)[CH2:22][CH2:21]4)[CH2:18][CH2:17]2)[CH2:12][CH:11]([OH:44])[CH:10]1[OH:45]

Participants

5

Procedure

1.5 g. cyclohexanone-helveticoside are dissolved in 20 ml. of 80% aqueous dioxane and treated dropwise over a period of 1 hour with a solution of 0.35 g. sodium borohydride in 20 ml. of 75% dioxane. The reaction mixture is stirred for 1 hour, after which no more cyclohexanone-helveticoside can be detected. The solution is adjusted to pH 7 with dilute sulfuric acid, and the dioxane is evaporated under reduced pressure in a rotating evaporator. The aqueous phase is extracted repeatedly with chloroform. The combined chloroform extracts are dried over anhydrous sodium sulfate and evaporated. The residue is purified chromatographically over silica gel, using chloroform as solvent. Yield: 750 mg. cyclohexanone-helveticosol. Melting point: 155°-164°C;[α D20 ] (C = 1, chloroform) : +23°.

Workup

  1. customthe dioxane is evaporated under reduced pressure in a rotating evaporator
  2. extractionThe aqueous phase is extracted repeatedly with chloroform
  3. dry with materialThe combined chloroform extracts are dried over anhydrous sodium sulfate
  4. customevaporated
  5. customThe residue is purified chromatographically over silica gel
  6. custom+23°

Sources & evidence

ORD record
ord-52086b9f38104f9aa7a4039dc6067098
Source dataset
uspto-grants-1976_04
Patent number
US03951946

Reaction notes

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