Carbamate → (1S,2S)-1-Amino-2-ethylcyclopropanecarboxylic acid

To carbamate 14c (267 mg, 0.810 mmol) was added a 1.0 M TBAF solution in THF (1.62 mL, 1.62 mmol, 2.0 eq.). The reaction mixture was stirred overnight at RT, refluxed for 30 min and then diluted with AcOEt. The solution was successively washed with water (2×) and brine. After the usual treatment (MgSO4, filtration and concentration) the desired amine 14d was isolated (122 mg, 0.721 mmol, 89% yield) as a pale yellow liquid. 1H NMR (CDCl3) δ5.94-5.86 (m,1H), 5.31-5.22 (m, 2H), 4.58 (d, J=5.7 Hz, 2H), 1.75 (bs, 2H), 1.61-1.53 (m, 2H), 1.51-1.42 (m, 2H), 1.00 (t, J=7.3 Hz, 3H), 0.70-0.62 (m, 1H).

1. temperaturerefluxed for 30 min
2. washThe solution was successively washed with water (2×) and brine
3. filtrationAfter the usual treatment (MgSO4, filtration and concentration) the desired amine 14d
4. customwas isolated (122 mg, 0.721 mmol, 89% yield) as a pale yellow liquid

ORD record

ord-ce0b4420a0874a2d9c35d4e2c646936c

Source dataset

uspto-grants-2010_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

USRE041894E1