6-Aminohexanoic Acid → 6-Aminocaproic acid N'-fmoc hydrazide

HRID 1081352Notes

Reaction equation

HRID 1081352 reaction equation
[CH2:1]([CH2:7][CH2:8][NH2:9])[CH2:2][CH2:3][C:4]([OH:6])=O.[C:10]([O:14][CH2:15][CH:16]1[C:28]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[C:22]2[C:17]1=[CH:18][CH:19]=[CH:20][CH:21]=2)(=[O:13])[NH:11][NH2:12]>>[C:10]([NH:11][NH:12][C:4](=[O:6])[CH2:3][CH2:2][CH2:1][CH2:7][CH2:8][NH2:9])([O:14][CH2:15][CH:16]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[C:22]2[C:17]1=[CH:18][CH:19]=[CH:20][CH:21]=2)=[O:13]

Participants

3

Reactant 2

HCID 5646-Aminohexanoic AcidHCID 1618839-Fluorenylmethyl carbazate

Product 1

HCID 587949346-Aminocaproic acid N'-fmoc hydrazide

Procedure

Using anhydrous conditions and under a nitrogen gas blanket, a 200 ml round bottom flask was charged with 4.90 g (10.48 mmol) of N-BOC-6-aminocaproic acid, N'-FMOC hydrazide, 8, and 10 ml of methylene chloride. The reaction mixture was then stirred at room temperature as 16 ml of trifluoroacetic acid (Schweizerhall) dissolved in 16 ml of methylene chloride was slowly added. The resultant homogeneous solution was allowed to stir for an additional 2 h and then 15 ml of toluene was added. The solvents and any remaining trifluoroacetic acid were then distilled off under reduced pressure. The distillation residue was twice more azeotroped with 15 ml portions of toluene to leave 8.49 g of orange oil. 1H NMR showed this crude material to contain the peaks associated with aminocaproic acid and a FMOC substituent. However, no tert-butyl peak was observed between 1-2 ppm showing removal of the BOC protecting group. This product was used without further purification.

Workup

  1. customremoval of the BOC protecting group
  2. customThis product was used without further purification

Sources & evidence

ORD record
ord-e1854d26d69041d482aa9a8747ce4dc1
Source dataset
uspto-grants-1996_12
Patent number
US05585468

Reaction notes

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