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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601737Generated: October 27, 2026

Sodium hydride → N-ethoxy-2-bromo-4-butyrolactam

https://huagongshe.com/reaction/601737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,4-dibromobutanoyl BromideHCID 11289826—
ReactantN-ethoxy-2,4-dibromobutyric acid amideHCID 86632273—
SolventBenzeneHCID 241—
ProductN-ethoxy-2-bromo-4-butyrolactamHCID 6727131337%

Reaction Steps

137 g of the above-obtained oil containing N-ethoxy-2,4-dibromobutyric acid amide were dissolved in 500 mL of benzene. To the resultant solution, 12 g of sodium hydride were gradually added while cooling the solution to 15° C. to 20° C. After the completion of the addition, ice was added to the resultant reaction solution to decompose excessive sodium hydride. The resultant solution was washed with a saturated saline, followed by drying the solution by magnesium sulfate. The solution was concentrated under a reduced pressure and purified by silica gel-acetone/benzene column chromatography to give 42 g (0.20 mol) of N-ethoxy-2-bromo-4-butyrolactam (with a yield of 37% from 2,4-dibromobutyric acid bromide).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902383B2
Source datasetuspto-grants-2011_03
ORD IDord-ef6711f74dbd46d0b64c017136d29623
Source noteuspto-grants-2011_03