Triethylamine → Benzyl cyclopropylcarbamate

HRID 252040Notes

Reaction equation

HRID 252040 reaction equation
[CH:1]1([NH2:4])[CH2:3][CH2:2]1.C(N(CC)CC)C.Cl[C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14]>ClCCl>[CH2:16]([O:15][C:13](=[O:14])[NH:4][CH:1]1[CH2:3][CH2:2]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 10387Benzyl chloroformate2×HCID 69828Cyclopropylamine

Product 1

HCID 13141013Benzyl cyclopropylcarbamateYield 587.7%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of cyclopropylamine (5.0 g, 87.5 mmol) and triethylamine (30 mL) in dichloromethane (100 mL) at 0° C. was added dropwise benzyl chloroformate (15.0 mL, 10.5 mmol) and the resulting mixture was stirred for 2 h. Additional benzyl chloroformate (1 mL) was added and the resulting reaction mixture was stirred overnight. The reaction was then quenched by addition of a saturated NaHCO3 and the separated aqueous phase was extracted several times with dichloromethane. The combined dichloromethane extracts were dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography (15% EtOAc to 5% MeOH/EtOAc) to give cyclopropyl-carbamic acid benzyl ester (11.8 g, 71%).

Workup

  1. customthe resulting reaction mixture
  2. stirringwas stirred overnight
  3. customThe reaction was then quenched by addition of a saturated NaHCO3
  4. extractionthe separated aqueous phase was extracted several times with dichloromethane
  5. dry with materialThe combined dichloromethane extracts were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by chromatography (15% EtOAc to 5% MeOH/EtOAc)

Sources & evidence

ORD record
ord-6c4a81913db049808bf7bdbf70da88dc
Source dataset
uspto-grants-2011_01
Patent number
US07868002B2

Reaction notes

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