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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352043Generated: November 2, 2026

Hydrochloric Acid → HCID 22661402, compound

https://huagongshe.com/reaction/1352043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
Reactant3-Amino-4,4,4-trifluorobutanoic acidHCID 342970—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22661402HCID 2266140247.5%

Reaction Steps

3-Amino-4,4,4-trifluorobutyric acid (10 g, 63.7 mmol) was added to a solution of sodium hydrogen carbonate (6.95 g, 82.8 mmol) in water (100 mL). A solution of 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy-2,5-pyrrolidinedione (Fmoc-Osu; 25.78 g, 76.4 mmol) in tetrahydrofuran (200 mL) was added. The solution was stirred at room temperature for 19 h and then acidified to pH 1 with 3 M HCl (250 mL). The mixture was extracted with ethyl acetate (250 mL then 100 mL) and the combined organic layers were washed with saturated brine (3×100 mL), dried (Na2SO4), filtered and concentrated to approximately 200 mL. Crystallization occurred on concentration. The mixture was allowed to stand for 10 min, then the solid was filtered off, washed with ethyl acetate and dried in a vacuum oven at 50° C. to give 3-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4,4,4-trifluorobutyric acid (11.47 g) as a white solid, mp 187–189° C. The mother liquor was concentrated to 80 mL. Crystallization occurred on concentration. The solid was filtered off, washed with ethyl acetate and dried in a vacuum oven at 50° C. to give a second batch of product (4.69 g). The overall yield was 16.16 g (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217728B2
Source datasetuspto-grants-2007_05
ORD IDord-5c4ca291862e450bad115d7a596e5982
Source noteuspto-grants-2007_05