Iodine → HCID 23295948, compound

HRID 964549Notes

Reaction equation

HRID 964549 reaction equation
[Mg].II.[CH2:4](Br)[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]=[CH2:14].Br[CH2:17][CH2:18][CH2:19][Cl:20].S(=O)(=O)(O)O>C1COCC1.[Cu](I)I>[CH2:19]([Cl:20])[CH2:18][CH2:17][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH:5]=[CH2:4]

Participants

8

Procedure

This example illustrates a synthesis for inventive compound no. 351 3. To a suspension of magnesium (1.86 g, 77.2 mmol) and a crystal of iodine in THF (20 ml) was added 10-undecenyl bromide (6.00 g, 25.8 mmol) in THF (14 m) over 40 minutes and the reaction stirred for a further 30 minutes after completion of the addition. The solution was added via a canula over 50 minutes to a suspension of copper iodide (0.50 g, 2.58 mmol) and 1-bromo-3-chloropropane (3.84 ml, 38.7 mmol) in THF (20 ml) and stirred at 25° C. for 16 hours. Sulfuric acid (1.0 M, 50 ml) was added, extracted with diethyl ether (2×60 ml) and the organic solvent was dried over magnesium sulfate and subsequently evaporated The residue was distilled at 0.25 mmHg, producing 3.06 g of 13-tetradecenyl chloride as a colorless liquid (51% yield, b.p. 98°-100° C.).

Workup

  1. customa synthesis for inventive compound no
  2. additionafter completion of the addition
  3. stirringstirred at 25° C. for 16 hours
  4. extractionextracted with diethyl ether (2×60 ml)
  5. dry with materialthe organic solvent was dried over magnesium sulfate
  6. customsubsequently evaporated The residue
  7. distillationwas distilled at 0.25 mmHg

Sources & evidence

ORD record
ord-f7432a83db764a4b9f959194dcf3dbd0
Source dataset
uspto-grants-1998_06
Patent number
US05770595

Reaction notes

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