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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173888Generated: November 3, 2026

Hydrochloric Acid → HCID 88540023, compound

https://huagongshe.com/reaction/2173888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Methoxycyclobutane-1-carboxylic acidHCID 22934762—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 88540023HCID 88540023—

Reaction Steps

Dichloromethane (20 mL) was added to the vial containing 3-methoxycyclobutanecarboxylic acid (1:1 isomers, 1500 mg, 11.53 mmol), N-methoxymethanamine.HCl (1514 mg, 15.53 mmol) and HATU (6570 mg, 17.3 mmol). Hunig's base (8.03 mL, 46.1 mmol) was then added. The mixture was stirred at room temperature overnight. The mixture was diluted with H2O and extracted with EtOAc three times. Insoluble solids were observed in the aqueous layer. The combined organic layers were washed with brined, dried over Na2SO4 and concentrated. The crude was dissolved in EtOAc and loaded to the column and purified by CombiFlash (40 g silica gel, EtOAc/heptane: 0→50%), leading to less polar diastereomer A and slightly more polar diastereomer B. Diastereomer A: 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 2.09-2.25 (m, 2H) 2.43-2.57 (m, 2H) 3.17 (s, 3H) 3.23 (s, 3H) 3.43 (m, 1H) 3.63 (s, 3H) 3.98-4.09 (m, 1H). GCMS: observed 173 for C8H15NO3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056834B2
Source datasetuspto-grants-2015_06
ORD IDord-dba35bc9a85040e9b170b95f2e7dab96
Source noteuspto-grants-2015_06