Methyl iodide → 2-(Methylthio)-4,5-dihydro-3h-1-benzazepine

HRID 1896145Notes

Reaction equation

HRID 1896145 reaction equation
[NH:1]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH2:5][CH2:4][CH2:3][C:2]1=[S:12].[OH-].[K+].I[CH3:16]>CC(C)=O>[CH3:16][S:12][C:2]1[CH2:3][CH2:4][CH2:5][C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N:1]=1

Participants

5

Procedure

A solution of Example 182B (2.3 g, 12.97 mmol) in acetone (51.9 mL) was heated to 60° C. in and oil bath. Then potassium hydroxide (36.4 g, 649 mmol) was added followed by the dropwise addition of iodomethane (0.811 mL, 12.97 mmol). The resulting yellow slurry was stirred for 5 minutes and then the solids were collected by filtration. The solids were washed with acetone and the filtrate was concentrated to obtain the crude title compound which was used was used without purification for the next reaction.

Workup

  1. filtrationthe solids were collected by filtration
  2. washThe solids were washed with acetone
  3. concentrationthe filtrate was concentrated

Sources & evidence

ORD record
ord-18195c565ff04e04bbbae462a1bbb29a
Source dataset
uspto-grants-2013_08
Patent number
US08518933B2

Reaction notes

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