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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176826Generated: November 2, 2026

HCID 68705549, compound → HCID 68703840, compound

https://huagongshe.com/reaction/1176826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68705549HCID 68705549—
ReactantHCID 178461633HCID 178461633—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68703840HCID 6870384081%

Reaction Conditions

Temperature120 °C

Reaction Steps

Heat CeCl3-7H2O (97 mg, 0.26 mmol) under vacuum at 70° C. for two hours and then warm slowly to 120° C. and continue heating overnight. Cool to room temperature and add THF (3 mL) followed by cyclopentanone 23 (100 mg, 0.26 mmol) and stir the solution for 45 minutes. Cool the reaction to −10° C., add EtMgCl (3.0 M in THF, 87 ul, 0.26 mmol) and stir the reaction for 30 minutes. Quench the reaction with saturated aqueous NH4 Cl and extract with EtOAc (2×), Combine the organic extracts, wash with brine, dry (Na2SO4), filter and concentrate. Purify by flash chromatography (10 g silica gel, 40 mL/min, dry loading on 700 mg of silica gel, 0-30% EtOAc/hexanes for 20 minutes and 30% EtOAe/hexanes for 13 minutes) to afford Alcohol 31 (86 mg, 0.207 mmol, 81%). 1H NMR (δ, 400 MHz, CDCl3) 7.36 (d, 2H, J=8.8 Hz), 7.05 (d, 2H, J=8.8 Hz), 6.90-6.87 (m, 2H), 6.83 (dd, 1H, J==8.8, 2.6 Hz), 5.19 (s, 2H) 5.14 (d, 1H,J=6.8 Hz), 5.10 (d, 1H, J=6.8 Hz), 5.05 (d, 1H, J=2.2 Hz), 3.54 (dd, 1H, J=7.6, 7.6 Hz), 3.51 (s, 3H), 3.49 (s, 3H), 2.70 (ddd, 1H, J=2.2, 7,6, 9.6 Hz), 2.22 (dd, 1H, J=13.6, 7.9 Hz), 2.03 (d, 1H, J=13.6 Hz), 1.84 (dd, 1H, J=14.1, 10.1 Hz), 1.67 (dd, 1H, J=14.1, 9.2 Hz), 1.52 (m, 2H), 0.89 (t, 3H, J=7.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842822B2
Source datasetuspto-grants-2010_11
ORD IDord-8d5903e293bd472cb881ee7deff749a9
Source noteuspto-grants-2010_11