Iodide Ion → HCID 54042371, compound

HRID 650856Notes

Reaction equation

HRID 650856 reaction equation
[CH2:1](I)[C:2]([CH3:5])([CH3:4])[CH3:3].[CH3:7][S:8](=[S:11])([O-:10])=[O:9].[Na+].[Al].[I-]>O.CN(C=O)C>[CH3:7][S:8](=[S:11])([O:10][CH2:1][C:2]([CH3:5])([CH3:4])[CH3:3])=[O:9]

Participants

7

Conditions

Temperature
90 °C

Procedure

The reaction mixture of neopentyl iodide (3.054 g, 0.0154 mol), sodium methanethiosulfonate (2.272 g, 0.0170 mol) and dry DMF (4 mL) was heated at 90° C. for 90 hr. The reaction flask was wrapped with aluminum foil to avoid direct sunlight to the reaction mixture, since the iodide was sensitive to sunlight. At the end of the heating, the reaction mixture was red-brown in color. At room temperature, water (15 mL) was added and the mixture was extracted with ether (3×30 mL). The combined ether extracts were washed twice with brine, dried, concentrated and the residue was subjected to column chromatography on silica gel with EtOAc-hexanes (1:2) to afford a colorless oil which slowly solidified (1.2395 g, 44%). The product was recrystallized from 95% EtOH. mp: 28.5-29.0° C.; IR (CH2Cl2 cast): 3021 (m), 2956 (m), 2868 (m), 1467 (m), 1433 (m), 1321 (st), 1310 (st), 1125 (st), 951 (m), 757 (m) and 724 cm−1 (m); 1H NMR (200 MHz, CDCl3): δ 3.32 (s, 3H, CH3SO2S), 3.13 (s, 2H, SCH2C), 1.05 (s, 9H, CMe3); 13C NMR (50 MHz, CDCl3): δ 50.23, 50.09, 32.14, 28.79, MS (El): 182 (M+), 57 (base peak, CMe3+).

Workup

  1. extractionthe mixture was extracted with ether (3×30 mL)
  2. washThe combined ether extracts were washed twice with brine
  3. customdried
  4. concentrationconcentrated
  5. customto afford a colorless oil which
  6. customThe product was recrystallized from 95% EtOH

Sources & evidence

ORD record
ord-697e2c7fbc5f43bebb2dfcff2d6c8433
Source dataset
uspto-grants-2001_08
Patent number
US06277617B1

Reaction notes

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