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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240257Generated: October 30, 2026

Ethylmorpholine → HCID 58031792, compound

https://huagongshe.com/reaction/240257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantDimethyl malonateHCID 7943—
ReactantMalonate IonHCID 9084—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant2-(3-TERT-BUTYLPHENOXY)PROPANOIC ACIDHCID 16770162—
SolventDimethylformamideHCID 6228—
ProductHCID 58031792HCID 5803179274%

Reaction Steps

To a solution of 250 mg (0.91 mmol) of dimethyl malonate, malonate, 314 mg (2.72 mmol) of N-ethylmorpholine, 153 mg (1.0 mmol) of HOBt hydrate and 155 mg (1.0 mmol) of EDAC in 7 ml of DMF was added a solution of 202 mg (0.91 mmol) of 2-(3-tert-butylphenoxy)propionic acid in 3 ml of DMF. After 18 h at room temperature, the reaction mixture was concentrated completely and separated by means of preparative HPLC (Merck Hibar Purospher Star RP-18e 10 μm 25×250 mm; A: H2O+0.05% TFA; B: ACN+0.05% TFA; flow rate: 50 ml/min; in 15 minutes 10% B→90% B). The product fractions were freeze-dried to give 323 mg (74%) of dimethyl 2-(1-{4-[2-(3-tert-butylphenoxy)propionylamino]phenyl}but-2-ynyl)malonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648038B2
Source datasetuspto-grants-2014_02
ORD IDord-e2a33a9e7c614756bacfb986dfeaf445
Source noteuspto-grants-2014_02