Hydrochloric Acid → HCID 10490193, compound

HRID 1472814Notes

Reaction equation

HRID 1472814 reaction equation
[Br-].[CH3:2][N:3]([CH3:25])[CH2:4][CH2:5][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Li]CCCC.[Br:31][C:32]1[CH:39]=[CH:38][C:35]([CH:36]=O)=[CH:34][CH:33]=1.Cl>O1CCCC1>[Br:31][C:32]1[CH:39]=[CH:38][C:35](/[CH:36]=[CH:5]/[CH2:4][N:3]([CH3:25])[CH3:2])=[CH:34][CH:33]=1

Participants

6

Conditions

Temperature
60 °C

Procedure

To a stirred solution of (2-dimethylaminoethyl)triphenylphosphonium bromide (1.12 g, 2.7 mmol) in tetrahydrofuran (10 ml) was added 2.5 M n-BuLi in hexanes (1.08 ml, 2.7 mmol) under nitrogen at 0° C. After 30 minutes 4-bromobenzaldehyde (0.5 g, 2.7 mmol) was added slowly and the reaction mixture was stirred at 60° C. overnight. The reaction mixture was acidified with 2M hydrochloric acid and extracted with toluene. The aqueous layer was then made alkaline with 2N sodium hydroxide and extracted twice with ethyl acetate. The organics were combined, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give the product as yellow oil. Yield 0.41 g, 63%. LCMS method: 2, RT: 2.62 min; MI: 240-242 [M+1].

Workup

  1. extractionextracted with toluene
  2. extractionextracted twice with ethyl acetate
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-c90bdb0bf3bf4846ba74e7a447580b3c
Source dataset
uspto-grants-2015_04
Patent number
US09012633B2

Reaction notes

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