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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453008Generated: October 31, 2026

HCID 58762434, compound → HCID 58762453, compound

https://huagongshe.com/reaction/1453008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58762434HCID 58762434—
ReactantHCID 178419650HCID 178419650—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58762453HCID 5876245372%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Cyclopentylmagnesium bromide (1.6 mL, 3.15 mmol, 2M soln in ether) was added to a cooled −78° C. solution of 3-Cyclohex-1-enyl-thiopropionic acid S-pyridin-2-yl ester (0.65 g, 2.63 mmol, from Step 3) dissolved in THF (10 mL). The reaction mixture was stirred for 45 min at −78° C. and then warmed up to rt. The reaction was quenched with 1N HCl and extracted with EtOAc. The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated. The residue was purified by silica gel chromatography (0% to 5% EtOAc in hexanes) to give the title compound as a clear oil (0.39 g, 72%). 1H NMR (CDCl3): δ 1.51-1.83 (br m, 12H), 1.91 (m, 2H), 1.97 (m, 2H), 2.20 (t, 2H, J=7.6 Hz), 2.54 (t, 2H, J=7.8 Hz), 2.87 (m, 1H), 5.39 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-2872d36e85d140009ee7c5b5a2d711bd
Source noteuspto-grants-2009_01