Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297238Generated: November 1, 2026

1,2-Dichloroethane → HCID 69515673, compound

https://huagongshe.com/reaction/1297238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 22182729HCID 22182729—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69515673HCID 69515673100.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(tert-butoxycarbonylamino-methyl)-2-isopropyl-cyclopropanecarboxylic acid (6.4 g, 24.9 mmol) in dry THF (190 mL) was added HOBt (4.7 g, 34.8 mmol), NMM (3.83 mL, 34.8 mmol) and EDC (6.7 g, 34.8 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 3 hours and quenched with concentrated ammonium hydroxide (16 mL). The reaction mixture was stirred at room temperature overnight. Excess of solvent was removed in vacuo and the residue was dissolved in EtOAc (200 mL). The organic layer was washed with 1N HCl, aqueous NaHCO3, brine and dried over Na2SO4. Evaporation of excess of solvent gave 6.4 g (100%) of (1-carbamoyl-2-isopropyl-cyclopropylmethyl)-carbamic acid tert-butyl ester as a colorless oil: 1H NMR (300 MHz, CD3OD) δ 0.62 (m, 1H), 1.00 (d, 3H), 1.05 (d, 3H), 1.25 (m, 3H), 1.45 (s, 9H), 3.05 (dd, 1H), 3.80 (dd, 1H), 6.70 (m, 1H); MS (APCI) m/z 257 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250433B2
Source datasetuspto-grants-2007_07
ORD IDord-422a9679d7a64f7eb308ca57004d430f
Source noteuspto-grants-2007_07