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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855644Generated: October 31, 2026

Myristyl bromide → HCID 25265779, compound

https://huagongshe.com/reaction/1855644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMyristyl bromideHCID 8208—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18373001HCID 18373001—
SolventEthanolHCID 702—
ProductHCID 25265779HCID 25265779—

Reaction Steps

3 g of 2, amino-1,3-propanediol were dissolved in 100 ml ethanol, 4 ml tetradecyl bromide were added followed by 5 ml diisopropyl ethylamine. The mixture was heated to reflux for 24 hours in a 250 ml round bottom flask equipped with a reflux condenser and stirred on a magnetic stirrer. The solution was evaporated to dryness and dissolved in 200 ml dichloromethane:methanol, 2:1, transferred to a 500 ml separatory funnel and washed with 75 ml 0.2N HCl. Phases were separated and the organic phase was washed again with 75 ml 0.1N HCl and 15 ml methanol. The organic phase was separated and dried on 5 g magnesium sulfate, filtered and evaporated to dryness. The resulted oil was crystallized from ethanol: H2O. Yield 1.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962891B2
Source datasetuspto-grants-2015_02
ORD IDord-da09787427064c9b81f9ec6496b6b300
Source noteuspto-grants-2015_02