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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301164Generated: October 31, 2026

Hydrochloric Acid → HCID 15158208, compound

https://huagongshe.com/reaction/2301164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantIsobutyl chloroformateHCID 62365—
ReactantCyclopentylacetic acidHCID 71606—
SolventDichloromethaneHCID 6344—
ProductHCID 15158208HCID 1515820883.7%

Reaction Steps

A solution of 2.0 mL (15.9 mmol) of cyclopentylacetic acid in 80 mL of CH2Cl2 at 0° C. was treated with 3.7 mL (33.6 mmol) of N-methyl-morpholine and 2.2 mL (16.9 mmol) of isobutyl chloroformate. After stirring for 20 min, 1.61 g (16.5 mmol) of N,O-dimethyl-hydroxylamine.HCl was added. The reaction was warmed to rt and stirred for 3 h. The reaction was partitioned between 200 mL of EtOAc and 200 mL 2.0 N HCl. After separating the phases, the organic layer was washed with 200 mL of 1.0 N NaHCO3, dried over Na2SO4 and concentrated. Flash chromatography on silica gel using 4:1 v/v hexanes/EtOAc afforded 2.28 g (83%) of the title compound as a colorless oil. RF: 0.27 (4:1 v/v hexanes/EtOAc). 1H NMR (300 MHz): δ 1.12-1.23 (m, 2H), 1.51-1.89 (m, 6H), 2.28 (m, 1H), 2.44 (d, J=7.5, 2H), 3.18 (s, 3H), 3.67 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498161B1
Source datasetuspto-grants-2002_12
ORD IDord-60258cf1322843fe9d0e0ce48e64d082
Source noteuspto-grants-2002_12