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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456853Generated: October 29, 2026

Hydrochloric Acid → HCID 178507187, compound

https://huagongshe.com/reaction/456853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178452622HCID 178452622—
SolventEthyl AcetateHCID 8857—
ProductHCID 178507187HCID 17850718731%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(nitroxy)butyric acid 4-[(2-tert-butoxycarbonylamino-3,5-dibromophenyl)methylamino]trans cyclohexyl ester (3.5 g, 5.74 mmoles) in ethyl acetate (100 ml), cooled at 0° C., a 5N HCl solution in ethyl acetate (5.95 ml) is added. The solution is maintained under stirring at 0° C. for 5 hours, then filtered. The obtained solid is suspended in ethyl acetate and the organic layer washed with a 5% sodium carbonate solution. The organic phase is washed with water, anhydrified with sodium sulphate and evaporated at reduced pressure. The residue is purified by chromatography on silica gel, eluting with n-hexane/ethyl acetate 1/1 (ratio by volume). 4-(nitroxy)butyric acid 4-[(2-amino-3,5-dibromophenyl) methylamino]trans cyclohexyl ester is obtained. Yield 31%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186753B1
Source datasetuspto-grants-2007_03
ORD IDord-c25bf76c719749fba743798f7e17ed2b
Source noteuspto-grants-2007_03