HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9331Generated: October 23, 2026
Benzyloxyamine hydrochloride → HCID 178419047, compound
https://huagongshe.com/en/reaction/9331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Reactant | 5'-Bromo-2'-(methylthio)spiro[cyclohexane-1,3'-[3H]indole] | HCID 21986266 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178419047 | HCID 178419047 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091234B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-2a5db7c4f64e47bcb8b812a4d9f7db0b |
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| Source note | uspto-grants-2006_08 |
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