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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236134Generated: October 25, 2026

Hexanoyl bromide → 2-Amino-3-methylpentanoic hexanoic anhydride

https://huagongshe.com/reaction/2236134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexanoyl bromideHCID 13226800—
ReactantSodium 2-amino-3-methylpentanoateHCID 23662724—
Product2-Amino-3-methylpentanoic hexanoic anhydrideHCID 25006169—

Reaction Steps

Finally, in a dry 2-necked, round bottomed flask, fixed with a separatory funnel, containing 10.81 g (60 mmol) of the prepared hexanoyl bromide, and side arm water condenser fixed with a dry receiving flask, is placed 11.03 g (72 mmol) of sodium 2-amino-3-methylpentanoate. The round bottomed flask is placed in an ice bath and the hexanoyl bromide is added drop wise. After addition is completed the mixture is shaken and the ice bath is replaced by a heating mantle. The flask is then heated until no more solution is dropping into the receiving flask. This crude distillate is then further fractionally distilled to yield 2-amino-3-methylpentanoic hexanoic anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714154B2
Source datasetuspto-grants-2010_05
ORD IDord-783a5e8823994034a12bed618e3ea0af
Source noteuspto-grants-2010_05