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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256043Generated: November 1, 2026

Ethyl Acetate → HCID 20164974, compound

https://huagongshe.com/reaction/256043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 20164896HCID 20164896—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 20164974HCID 20164974—

Reaction Steps

To a suspension of 3.4 g of 2-(1-naphthyl)-5-oxo-6-phthalimidoperhydro-1,4-thiazepine [prepared as described in step (e) above] in a mixture of 34 ml of dimethylformamide and 10 ml of hexamethylphosphoric triamide were added dropwise 2.25 ml of t-butyl bromoacetate and then, bit by bit, 609 mg of a 55% w/w suspension of sodium hydride in oil at 0°-5° C., under a nitrogen stream. After this addition, the reaction mixture was stirred for 16 hours at room temperature. Ethyl acetate and water were then added to the reaction mixture. The ethyl acetate layer was separated, washed with water and dried over anhydrous magnesium sulfate, and the solvnet was distilled off. The residue was subjected to silica gel column chromatography using a 2:1 by volume mixture of cyclohexane and ethyl acetate as eluent, to give 2.6 g of the title compound as crystals, melting at 211°-213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699905
Source datasetuspto-grants-1987_10
ORD IDord-1c76f7cdeb1d4f10bd0141c957fddec4
Source noteuspto-grants-1987_10