Ethanol → HCID 86755072, compound

HRID 849804Notes

Reaction equation

HRID 849804 reaction equation
C(OCC)C.[H-].[H-].[H-].[H-].[Li+].[Al+3].C([O:14][C:15](=O)[CH2:16][C:17]1([CH2:37][C:38](O)=[O:39])[S:21][C:20]2[CH:22]=[C:23]3[S:27][C:26]([CH2:32][C:33](O)=[O:34])([CH2:28][C:29](O)=[O:30])[S:25][C:24]3=[CH:36][C:19]=2[S:18]1)C.C(O)C>O>[OH:34][CH2:33][CH2:32][C:26]1([CH2:28][CH2:29][OH:30])[S:25][C:24]2[CH:36]=[C:19]3[S:18][C:17]([CH2:37][CH2:38][OH:39])([CH2:16][CH2:15][OH:14])[S:21][C:20]3=[CH:22][C:23]=2[S:27]1

Participants

6

Procedure

A dry flask under argon atmosphere was charged with diethyl ether (2600 ml) and LiAlH4 (21.2 g 0.56 mol) Benzo[1,2-d:4,5-d']bis(1,3)dithiole-2,2,6,6-tetraacetic acid ethyl ester (80.2 g, 0.139 mol) was added and the mixture was refluxed for 26 h. The mixture was cooled to ambient temperature and ethanol (165 ml) was carefully added followed by water (410 ml). The ether was decanted off and the white precipitate was stirred with water (3300 ml) to give a slurry. After acidification with hydrochloric acid the slurry was filtered and the crude product was washed with water and dried.

Workup

  1. additionwas added
  2. temperaturethe mixture was refluxed for 26 h
  3. customThe ether was decanted off
  4. customto give a slurry
  5. filtrationAfter acidification with hydrochloric acid the slurry was filtered
  6. washthe crude product was washed with water
  7. customdried

Sources & evidence

ORD record
ord-e7f256163e2045f38bc8f035fe9f3724
Source dataset
uspto-grants-2000_01
Patent number
US06013810

Reaction notes

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