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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230804Generated: October 26, 2026

Hydrogen Bromide → Bromosuccinic acid, (-)-

https://huagongshe.com/reaction/2230804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantL-Aspartic AcidHCID 5960—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductBromosuccinic acid, (-)-HCID 275718151%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a 500 mL round bottom flask was added L-aspartic acid ((S)-aspartic acid, 25 g, 188 mmol) and 245 mL of 5 N HBr. The reaction was cooled in an ice bath to 0-50° C., followed by the dropwise addition of sodium nitrite (20.7 g, 301 mmol) in 75 mL of water over five hours. The temperature was maintained below 50° C. during the addition. After the addition was complete, the reaction was allowed to stir for 12 hours at 23-25° C. The reaction was diluted with diethyl ether (120 mL). The aqueous layer was removed and the organic phase was washed with 1 N HCl (100 mL). The combined aqueous phases were washed with EtOAc (100 ml). The combined organic extracts were dried (MgSO4), filtered and concentrated under reduced pressure to leave the product as a slightly yellow solid. The solid was recrystallized from EtOAc (˜100 mL) and hexanes (˜10 mL) to obtain the product (19.03 g, 97 mmol, 51%) as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426357B1
Source datasetuspto-grants-2002_07
ORD IDord-3f1592df85c045c1a29780df9b554ea9
Source noteuspto-grants-2002_07