Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360550Generated: November 1, 2026

1,2-Dichloroethane → HCID 24744642, compound

https://huagongshe.com/reaction/2360550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPhenethylamineHCID 1001—
ReactantDimethylformamideHCID 6228—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant8-(tert-Butoxycarbonyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxylic acidHCID 11414901—
SolventEthyl AcetateHCID 8857—
ProductHCID 24744642HCID 24744642—

Reaction Steps

To a solution of 8-(tert-butoxycarbonyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxylic acid (300 mg, 1.06 mmol), EDC (242 mg, 1.26 mmol), HOBt (171 mg, 1.26 mmol) in DMF (4 mL) was added phenethylamine (159 mL, 1.26 mmol). After 4 h at room temperature, the reaction mixture was diluted with EtOAc (10 mL) and washed with H2O (1×5 mL) and brine (1×5 mL). The organic layer was dried over Na2SO4, filtered, and concentrated. The crude oil was taken up in CH2Cl2 (4 mL) and treated with TFA (2 mL). The reaction mixture was concentrated and the crude oil purified by reverse-phase chromatography (10-75% MeCN/H2O with 0.05% TFA) to give the N-(2-phenylethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxamide confirmed by MS (ESI+): cal'd [M+H]+ 288.2, obs'd 288.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686020B2
Source datasetuspto-grants-2014_04
ORD IDord-0642eabaef1f4a1b9bb0c792db526afb
Source noteuspto-grants-2014_04