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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771061Generated: November 4, 2026

Hydrochloric Acid → 11-Carboxyundecyl 5-amino-4-oxopentanoate hydrochloride

https://huagongshe.com/reaction/1771061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant11-carboxyundecyl 5-(Boc-amino)-4-oxopentanoateHCID 90034503—
SolventEthyl AcetateHCID 8857—
Product11-Carboxyundecyl 5-amino-4-oxopentanoate hydrochlorideHCID 90034489—

Reaction Steps

A 1.0 M solution of HCl in diethyl ether (5.0 mL; 5.0 mmol) was added to a stirred solution of the product of 14c (0.95 g; 2.2 mmol) in ethyl acetate (10 mL) at ambient temperature under argon. After 5 days, the mixture was filtered and the residue was triturated with diethyl ether (2×5 mL). The residue was dried overnight at 40° C. and 15 mm Hg to give 0.11 g white solid. The combined ether extracts were evaporated. LC-MS analysis indicated that the product contained ca. 25% 5-amino-4-oxopentanoic acid; the combined crops were purified by flash chromatography on a 150×25 mm silica gel 60 column eluted sequentially with 3% methanol in acetonitrile (1000 mL), 6% methanol in acetonitrile (1000 mL), then 9% methanol in acetonitrile (2000 mL), collecting 56×50 mL fractions. Fractions containing the product were evaporated and the residue was dissolved in water (10 mL). The solution was freeze-dried overnight, and 0.06 g (7.5%) product obtained (white solid, mp 110-115° C. (softens, no sharp mp)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249086B2
Source datasetuspto-grants-2016_02
ORD IDord-801e50831b014a2bbbafa8f41e5929b3
Source noteuspto-grants-2016_02