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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167387Generated: November 3, 2026

Ethyl 2-(diphenylmethyleneamino)acetate → HCID 15610108, compound

https://huagongshe.com/reaction/1167387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 15610108HCID 1561010899.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of N-(diphenylmethylene)glycine ethyl ester (available from Aldrich Chemical Co., Milwaukee, Wis.) (50.0 g, 187 mmol) in dry THF (200 mL) at −78° C. under argon was added a 1.0 M solution of lithium bis(trimethylsilyl)amide (Li HMDS; 210 mL, 0.2 mol) in THF over a period of 45 min (“1.A, Scheme A). After 0.5 hour at −78° C., 3-bromo-2-methylpropene (18.91 mL, 187 mmol) was added dropwise to the orange-yellow suspension. After the addition was complete, the reaction mixture was stirred for an additional 0.5 hour at 0° C. and then allowed to warm to room temperature. After 1 hour the reaction mixture was concentrated under reduced pressure to give an orange-colored oil. The crude material was dissolved in ethyl acetate (EA) (600 mL), washed with brine (100 mL), dried over anhydrous MgSO4 and concentrated under reduced pressure to give the desired compound (60 g, 99%), which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617426B1
Source datasetuspto-grants-2003_09
ORD IDord-f1ae02f00ffc4d03bb59f65066cfaad9
Source noteuspto-grants-2003_09