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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786285Generated: October 31, 2026

Methyl (8-methyl-8-azabicyclo[3.2.1]octan-3-ylidene)acetate → HCID 11484351, compound

https://huagongshe.com/reaction/1786285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (8-methyl-8-azabicyclo[3.2.1]octan-3-ylidene)acetateHCID 13670649—
ReactantHCID 178418439HCID 178418439—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductAmmonium HydroxideHCID 149232%
ProductHCID 11484351HCID 1148435178.1%

Reaction Steps

A solution of (8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-acetic acid methyl ester (200 mg, 1.02 mmol) in THF (3 mL) was mixed with 2-thienyllithium (2.02 mL, 1.0 M in THF, 2.02 mmol). The mixture was stirred overnight at r.t., diluted with saturated NH4Cl aqueous solution (20 mL) and extracted with EtOAc. The combined organic phases were dried over MgSO4 and concentrated. Flash chromatography (90% CH2Cl2, 8% CH3OH, 2% NH4OH) then afforded the title compound (132 mg, 39%): LCMS (ES) m/z 332 (M+H)+; 1H-NMR(MeOD) δ 1.35 (m, 1H), 1.61 (m, 1H), 1.81 (m, 1H), 1.95 (m, 1H), 2.12 (m, 3H), 2.29 (s, 3H), 2.37 (m, 1H), 2.68 (m, 1H), 3.03 (m, 1H), 3.22 (m, 1H), 3.32 (s, 1H), 6.15 (s, 1H), 6.95 (m, 4H), 7.30 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507747B2
Source datasetuspto-grants-2009_03
ORD IDord-4c3711d37de04af6b2801673c3f820ea
Source noteuspto-grants-2009_03