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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849441Generated: October 25, 2026

Hydrochloric Acid → Fmoc-L-aspartic acid

https://huagongshe.com/reaction/849441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-Aspartic AcidHCID 5960—
ReactantSodium CarbonateHCID 10340—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductFmoc-L-aspartic acidHCID 701901671%

Reaction Steps

Forty-five g (0.134 M, 0.96 eq) of Fmoc-Osu was added to 20 g (0.15 M, 1 eq) of aspartic acid and 20 g of Na2CO3 dissolved in 400 mL of water and 200 mL of dioxane. The mixture was stirred for 2 hrs while the pH was maintained at about 9 by the addition of small amounts of Na2CO3. Then the cloudy white mixture was poured into 500 mL of ice water containing 40 mL of conc HCl. The white solid was extracted with 500 mL EtOAc and this was mixed with 500 mL of hexane. The mixture was chilled overnight and stirred the next day to give 38 g of Fmoc-aspartic acid as crystals (71% yield) upon filtration and air drying. 10 g (0.28 M) of this product was dissolved in 200 mL of methanol and 20 mL of conc H2SO4 was added. The solution was allowed to stand overnight. The mixture was poured into 1 L of water and filtered. The resulting white solid was dried and redissolved in EtOAc. Slow addition of hexane and chilling gave 9 g (83% yield) of product as white needles, mp 78-80°. [a]d =-13.9°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013462
Source datasetuspto-grants-2000_01
ORD IDord-f6a1b5ec6e01497988ae1d8233045995
Source noteuspto-grants-2000_01