HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691659Generated: October 27, 2026
Trifluoroacetic acid → 3-(2-Methoxy-5-nitrobenzyl)-8-(3-phenoxypropyl)-1-oxa-3,8-diazaspiro[4.5]decan-2-one
https://huagongshe.com/reaction/1691659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzene, (3-bromopropoxy)- | HCID 68522 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(2-Methoxy-5-nitrobenzyl)-2-oxo-1-oxa-3,8-diazaspiro[4.5]decane-8-carboxylic acid tert-butyl ester | HCID 57666278 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2-Methoxy-5-nitrobenzyl)-8-(3-phenoxypropyl)-1-oxa-3,8-diazaspiro[4.5]decan-2-one | HCID 11992223 | — |
Reaction Steps
Compound A8 (0.67 g, 1.59 mmol) was dissolved in DCM (3 mL) and combined with trifluoroacetic acid (3 mL). The reaction mixture was stirred for 5 min at RT and the solvent was then removed under a vacuum. The residue was combined repeatedly with toluene and the solvent was then removed again. The residue was then combined with sat. aq. NaHCO3 solution and repeatedly extracted with EtOAc. The combined organic phases were dried over Na2SO4 and the solvent was removed under a vacuum. The residue was redissolved in anhydrous THF (5 mL) and combined with diisopropylethylamine (333 μL, 1.91 mmol). The reaction mixture was combined with 3-phenoxypropyl bromide (277 μL, 1.75 mmol), stirred for 18 h at RT and combined with water and EtOAc. The organic phase was separated off and the aqueous phase repeatedly extracted with EtOAc. The combined organic phases were dried over Na2SO4 and the solvent was removed under a vacuum. The residue was purified by column chromatography (SiO2, DCM/MeOH 98:2). 433 mg (58% of theoretical) of the desired product 3-(2-methoxy-5-nitrobenzyl)-8-(3-phenoxypropyl)-1-oxa-3,8-diazaspiro[4.5]decan-2-one (432) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153795B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-c4e333a6d9774a5e825a78eafcb4dcc6 |
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| Source note | uspto-grants-2012_04 |
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