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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838760Generated: November 2, 2026

Sodium hydride → HCID 20820309, compound

https://huagongshe.com/reaction/1838760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 575184HCID 575184—
SolventDimethylformamideHCID 6228—
ProductHCID 20820309HCID 20820309—

Reaction Steps

3.3 g of perhydro-1,5-diazocin-2,6-dione are suspended in 30 ml of absolute DMF, and 732 mg of sodium hydride (80%) are then added. The mixture is stirred at RT for 15 min and then cooled to 0° C., and 3.76 ml of tert-butyl bromoacetate are then added. The mixture is stirred at 0° C. for 15 min and at RT for 30 min, and is then once again cooled to 0° C., and another 732 mg of sodium hydride (80%) are added. After 15 min, a further 3.76 ml of tert-butyl bromoacetate are added using a pipette, the ice bath is removed after 15 min and the mixture stirred at RT overnight. The mixture is then diluted with dichloromethane, water is added, and the phases are then separated and the organic phase is washed twice with water. The organic phase is dried over MgSO4 and concentrated, and the residue is dried under high vacuum and recrystallized from n-hexane. This gives 2.5 g of the title compound of m.p. 180° C. The mass spectrum shows the molecular peaks MH+ and MNH4+ at 371 and 388 Da.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673786B1
Source datasetuspto-grants-2004_01
ORD IDord-01501605a2b04ce8bb8272ea38b6e5f8
Source noteuspto-grants-2004_01