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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201080Generated: October 29, 2026

1,2-Dichloroethane → HCID 59199861, compound

https://huagongshe.com/reaction/2201080

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(R)-2-((tert-Butoxycarbonyl)amino)-3-cyclopropylpropanoic acidHCID 2756015—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59199861HCID 59199861—

Reaction Steps

To a solution of above mentioned (R)-2-(tert-butoxycarbonylamino)-3-cyclopropylpropanoic acid (1.0 g, 4.36 mmol) in DMF (10 ml) was added EDC (1.0 g, 5.24 mmol) and HOBt.H2O (367 mg, 2.4 mmol) at room temperature, 20 min later, it was added ammonia in MeOH (7N, 0.6 mL, 4 mmol) at room temperature. After stirring for 30 min, it was diluted with water and EtOAc, organic layer was separated and washed with Sat. NaHCO3, brine, dried and concentrated to give (R)-tert-butyl-1-amino-3-cyclopropyl-1-oxopropan-2-ylcarbamate (750 mg) as crude oil, which was treated with 4N HCl in Dioxane (5 mL). 30 min later, it was concentrated to give (R)-2-amino-2-cyclopropylacetamide hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359375B2
Source datasetuspto-grants-2016_06
ORD IDord-2416f999230e4d3f87b6f3371efd7a89
Source noteuspto-grants-2016_06