Hydrochloric Acid → HCID 21865156, compound

HRID 1365883Notes

Reaction equation

HRID 1365883 reaction equation
N[C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH3:15])([CH3:14])[CH2:7][N:8]2[C:11](=[O:13])[CH3:12])=[CH:4][CH:3]=1.Cl.N([O-])=O.[Na+].[I-:21].[K+]>O.C(Cl)Cl>[I:21][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH3:15])([CH3:14])[CH2:7][N:8]2[C:11](=[O:13])[CH3:12])=[CH:4][CH:3]=1

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 4875Potassium IodideHCID 218651761-(6-Amino-3,3-dimethylindolin-1-yl)ethanoneHCID 23668193Sodium Nitrite

Product 1

HCID 21865156HCID 21865156, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolvent3×HCID 6344DichloromethaneSolvent

Procedure

To a suspension of 1-(6-amino-3,3-dimethylindolin-1-yl)ethanone (2.000 g, 9.791 mmol) in concentrated HCl (20.00 ml, 548.5 mmol) at 0° C. was added ice (15 g) followed by a solution of sodium nitrite (0.7769 g, 11.26 mmol) in water (15 mL). After 45 min, a solution of potassium iodide (3.251 g, 19.58 mmol) in water (15 mL) was added dropwise. After 5 min, the mixture was allowed to warm to RT. After 1 hr, CH2Cl2 (ca. 100 mL) and water (ca. 25 mL) were added. The aqueous fraction was extracted 2× with DCM. The combined organic fractions were washed with saturated NaHCO3 followed by 10% NaS2O3 and brine. After drying with Na2SO4, the deep red solution was concentrated in vacuo and purified by silica gel chromatography using 10-60% hexanes:EtOAc to afford 1-(6-iodo-3,3-dimethylindolin-1-yl)ethanone as an orange oil that solidified upon standing.

Workup

  1. waitAfter 5 min
  2. waitAfter 1 hr
  3. extractionThe aqueous fraction was extracted 2× with DCM
  4. washThe combined organic fractions were washed with saturated NaHCO3
  5. dry with materialAfter drying with Na2SO4
  6. concentrationthe deep red solution was concentrated in vacuo
  7. custompurified by silica gel chromatography

Sources & evidence

ORD record
ord-dda7a12638774b0890cbae61442581ed
Source dataset
uspto-grants-2011_02
Patent number
US07893061B2

Reaction notes

Loading…