[4-(4-Nitrophenyl)but-3-ynyl]carbamic acid tert-butyl ester → [4-(4-Aminophenyl)butyl]carbamic acid tert-butyl ester

HRID 1795040Notes

Reaction equation

HRID 1795040 reaction equation
[C:1]([O:5][C:6](=[O:21])[NH:7][CH2:8][CH2:9][C:10]#[C:11][C:12]1[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][CH:13]=1)([CH3:4])([CH3:3])[CH3:2]>C(O)C.[Pd]>[C:1]([O:5][C:6](=[O:21])[NH:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[CH:13]=[CH:14][C:15]([NH2:18])=[CH:16][CH:17]=1)([CH3:4])([CH3:2])[CH3:3]

Participants

4

Reactant 1

HCID 11716220[4-(4-Nitrophenyl)but-3-ynyl]carbamic acid tert-butyl ester

Product 1

HCID 11558019[4-(4-Aminophenyl)butyl]carbamic acid tert-butyl esterYield 96%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

To a solution of compound 51 (2.01 g, 6.923 mmol) in ethanol (50 mL) was added 10% palladium on carbon (737 mg, wet) in one portion under argon protection. The flask was evacuated and re-filled with argon three times (to remove oxygen), and the mixture stirred at room temperature overnight under one atmosphere of hydrogen. The reaction system was then purged with nitrogen, and the catalyst was vacuum filtered and washed with ethanol (2×5 mL). The filtrate and washings were combined and concentrated under reduced pressure. The residue was chromatographed over silica gel, eluting with a mixture of ethyl acetate (0–25%) and hexanes (100–75%), to afford 1.75 g (96%) of the product 52 as a colorless viscous oil. 1H NMR (CDCl3) δ 1.44 (s, 9H), 1.47–1.64 (m, 4H), 2.50 (t, J=7.1 Hz, 2H), 3.08–3.14 (m, 2H), 3.57 (br s, 2H), 4.55 (br s, 1H), 6.62 (d, J=8.2 Hz, 2H), 6.95 (d, J=8.2 Hz, 2H). m/z (APCI)=265 [C15H24N2O2+H]+.

Workup

  1. customThe flask was evacuated
  2. additionre-filled with argon three times (to remove oxygen)
  3. customThe reaction system was then purged with nitrogen
  4. filtrationfiltered
  5. washwashed with ethanol (2×5 mL)
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was chromatographed over silica gel
  8. washeluting with a mixture of ethyl acetate (0–25%) and hexanes (100–75%)

Sources & evidence

ORD record
ord-9637c0c171764fd0bae00ac30af54d0a
Source dataset
uspto-grants-2006_04
Patent number
US07026325B2

Reaction notes

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