Hydrochloric Acid → 2-[(2,2,2-Trifluoroacetyl)amino]hexanoic acid

HRID 2357110

Reaction equation

HRID 2357110 reaction equation
[CH2:1]([CH2:7][CH2:8]N)[CH2:2][CH2:3][C:4]([OH:6])=[O:5].C([N:12](CC)CC)C.[F:17][C:18]([F:25])([F:24])[C:19](OCC)=[O:20].Cl>CO>[F:17][C:18]([F:25])([F:24])[C:19]([NH:12][CH:3]([CH2:2][CH2:1][CH2:7][CH3:8])[C:4]([OH:6])=[O:5])=[O:20]

Participants

6

Procedure

ω-aminocaproic acid (2.59 g, 19.7 mol) was dissolved in 100 mL methanol, and triethylamine (4.2 mL, 29.9 mmol) and ethyl trifluoroacetate (3.5 mL, 29.5 mmol) were added and agitated for a day and night at room temperature. The reaction solution was poured into 1% by weight hydrochloric acid (100 mL), and extracted once with methylene chloride. The methylene chloride layer was washed once with water and once with a saturated aqueous sodium chloride solution, and then dried and concentrated with anhydrous sodium sulfate to obtain 2.78 g of a crude product.

Workup

  1. extractionextracted once with methylene chloride
  2. washThe methylene chloride layer was washed once with water and once with a saturated aqueous sodium chloride solution
  3. customdried
  4. concentrationconcentrated with anhydrous sodium sulfate

Sources & evidence

ORD record
ord-c5c898a5e9244e74aa6e3c0d887164ce
Source dataset
uspto-grants-2010_07
Patent number
US07759473B2

Linked notes

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