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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173155Generated: October 31, 2026

1,2-Dichloroethane → HCID 86633507, compound

https://huagongshe.com/reaction/1173155

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPhenethylamineHCID 1001—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant8-(tert-Butoxycarbonyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxylic acidHCID 11414901—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86633507HCID 86633507—

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 μL, 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 N2-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 numberUS07834026B2
Source datasetuspto-grants-2010_11
ORD IDord-c6c02b0930104558b45960e4df65f0b3
Source noteuspto-grants-2010_11