Réaction #632004

Équation de réaction

2-trimethylsilyl-ethanol

triethylamine

DPPA

product

racemic 2-Ethylcyclopropane-1,1-dicarboxylic acid tert-butyl ester

→

desired product

(1S,2S) 2-ethyl-1-(2-trimethylsilanylethoxycarbonylamino)cyclopropane-carboxylic acid tert-butyl ester

Solvants

benzene

Conditions de réaction

Traitement

1. 1
   TempératureThe reaction mixture was heated
2. 2
   Températureto reflux for 3.5 hours
3. 3
   Températureheated
4. 4
   Températureto reflux overnight
5. 5
   FiltrationThe reaction mixture was filtered
6. 6
   workup.ADDITIONdiluted with diethyl ether
7. 7
   Lavagewashed sequentially with 10% aqueous citric acid solution, water, saturated aqueous NaHCO3, water (2×), and brine (2×)
8. 8
   Séchagedried (MgSO4)
9. 9
   Filtrationfiltered
10. 10
    Concentrationconcentrated in vacuo
11. 11
    Filtrationfiltered

Mode opératoire

To a suspension of the product of Step 2 (10 g, 46.8 mmol) and 3 g of freshly activated 4 Å molecular sieves in dry benzene (160 mL) was added triethylamine (7.50 mL, 53.8 mmol) and DPPA (11 mL, 10.21 mmol). The reaction mixture was heated to reflux for 3.5 hours, treated with 2-trimethylsilyl-ethanol (13.5 mL, 94.2 mmol), and heated to reflux overnight. The reaction mixture was filtered, diluted with diethyl ether, washed sequentially with 10% aqueous citric acid solution, water, saturated aqueous NaHCO3, water (2×), and brine (2×), dried (MgSO4), filtered, and concentrated in vacuo. The residue was suspended with 10 g of Aldrich polyisocyanate scavenger resin in 120 mL of dichloromethane, stirred at room temperature overnight, and filtered to provide the desired product (8 g, 24.3 mmol; 52%) as a pale yellow oil: 1H NMR (CDCl3) δ 0.03 (s, 9H), 0.97 (m, 5H), 1.20 (br m, 1H), 1.45 (s, 9H), 1.40-1.70 (m, 4H), 4.16 (m, 2H), 5.30 (br s, 1H).

Source