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Diethyl Ether → HCID 50914394, compound

HRID 1895527
Notes
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Reaction equation

HRID 1895527 reaction equation
C([Li])(C)(C)C.I[C:7]1([CH2:10][C@H:11]2[CH2:15][O:14][C:13]([CH3:17])([CH3:16])[O:12]2)[CH2:9][CH2:8]1.[S:18]([Cl:21])(Cl)=[O:19].CC[O:24]CC>>[CH3:16][C:13]1([CH3:17])[O:12][C@@H:11]([CH2:10][C:7]2([S:18]([Cl:21])(=[O:19])=[O:24])[CH2:9][CH2:8]2)[CH2:15][O:14]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 3283Diethyl Ether2×HCID 24386Thionyl ChlorideHCID 66849166HCID 66849166, compoundHCID 178418306HCID 178418306, compound

Product 1

HCID 50914394HCID 50914394, compound

Conditions

Temperature
-78 °C

Procedure

tert-Butyl lithium (2 eq) is added to a solution of (S)-4-((1-iodocyclopropyl)methyl)-2,2-dimethyl-1,3-dioxolane (1 eq) in ether at −78° C. and the mixture stirred at −78° C. for 30 mins. A solution of thionyl chloride in ether is added, the mixture warmed to room temperature and concentrated under reduced pressure. The residue is dissolved in chloroform, filtered and dried under reduced pressure.

Workup

  1. temperaturethe mixture warmed to room temperature
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe residue is dissolved in chloroform
  4. filtrationfiltered
  5. customdried under reduced pressure

Sources & evidence

ORD record
ord-26d684c43209428f88139d9d1ddf2e76
Source dataset
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08513443B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes