Acetic Anhydride → HCID 18923997, compound

HRID 54833Notes

Reaction equation

HRID 54833 reaction equation
[O:1]1[C:5]2([CH2:10][CH2:9][S:8](=O)[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.C(OC(=O)C)(=[O:14])C.N1C(C)=CC=CC=1C>C(OCC)(=O)C>[O:1]1[C:5]2([CH2:10][CH2:9][S:8][CH:7]([OH:14])[CH2:6]2)[O:4][CH2:3][CH2:2]1

Participants

5

Conditions

Temperature
150 °C

Procedure

A mixture of 0.88 g of product from Example 393, 5.0 ml of acetic anhydride and 2.0 ml of lutidine is heated at 110°-115° C. for 2.5 hours, followed by increasing the temperature to 150° C. and then heated for 3 hours. The reaction mixture is diluted with ethyl acetate, washed 2× with 1N hydrochloric acid, water, saturated sodium chloride, dried and concentrated in vacuo. The residue is dissolved in methylene chloride, filtered through a pad of hydrous magnesium silicate and reconcentrated in vacuo to give 0.569 g of the desired product.

Workup

  1. temperatureis heated at 110°-115° C. for 2.5 hours
  2. temperatureheated for 3 hours
  3. washwashed 2× with 1N hydrochloric acid, water, saturated sodium chloride
  4. customdried
  5. concentrationconcentrated in vacuo
  6. dissolutionThe residue is dissolved in methylene chloride
  7. filtrationfiltered through a pad of hydrous magnesium silicate

Sources & evidence

ORD record
ord-4a19366506b44ae3b000b9462a40cb26
Source dataset
uspto-grants-1997_04
Patent number
US05623081

Reaction notes

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