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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760306Generated: October 25, 2026

Benzyloxyamine hydrochloride → HCID 178419047, compound

https://huagongshe.com/reaction/1760306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxyamine hydrochlorideHCID 102312—
Reactant5'-Bromo-2'-(methylthio)spiro[cyclohexane-1,3'-[3H]indole]HCID 21986266—
SolventMethanolHCID 887—
ProductHCID 178419047HCID 178419047—

Reaction Conditions

Temperature45 °C

Reaction Steps

5′-Bromo-2′-(methylthio)spiro[cyclohexane-1,3′-[3H]indole] (9.0 g, 28.98 mmol) and O-benzylhydroxylamine hydrochloride (13.8 g, 86.9 mmol) were combined in methanol (150 mL) and heated to 45° C. for 6 hours. Methanol was evaporated in vacuo. Ethyl acetate was added to the residue and this mixture was washed with ammonium chloride solution. Ethyl acetate was dried over magnesium sulfate, ethyl acetate collected evaporated in vacuo and the residue was flash chromatographed on alumina 90 (9:1 Hexane/EtOAc) to the desired product (6.5 g, 60%). 1H NMR (DMSO-d6, 300 MHz) δ 1.38-1.70 (m, 8H), 1.92-2.06 (m, 2H), 5.06 (s, 2H), 6.71 (d, 1H, J=8.26 Hz), 7.22-7.43 (m, 7H), 9.62 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841568B2
Source datasetuspto-grants-2005_01
ORD IDord-7630809d26984c49b8c2e33ab7d3a407
Source noteuspto-grants-2005_01