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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202141Generated: November 4, 2026

HCID 68315186, compound → HCID 67207079, compound

https://huagongshe.com/reaction/2202141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68315186HCID 68315186—
ReactantHCID 68315188HCID 68315188—
ReactantHCID 86671523HCID 86671523—
CatalystHCID 178418397HCID 178418397—
ProductHCID 67207079HCID 67207079—

Reaction Steps

The title compound was prepared by the general procedure described for compound 11a (HU-911), using pinacol arylboronate 4 (mixed with 2) 0.244 g, enol triflate 9a 0.2 g (0.61 mmol), Pd(PPh3)4 0.042 g (0.037 mmol) and t-BuNF 0.91 ml (0.91 mmol, 1M solution in THF) to give colorless oil 170 mg (72%). 1H NMR (300 MHz, CDCl3) δ ppm 6.33 (s, 2H), 6.26 (d, J=3.42 Hz, 1H), 3.71 (s, 6H), 3.47 (s, 3H), 2.55 (t, J=7.70 Hz, 2H), 2.38-2.46 (m, 2H), 1.81-2.03 (m, 2H), 1.56-1.66 (m, 2H), 1.30-1.35 (m, 4H), 1.12 (s, 3H, syn), 1.07-1.16 (m, 1H), 0.97 (s, 3H, anti), 0.90 (t, J=6.84 Hz, 3H). Exact mass calculated for C24H34O4 by the general procedure described for compo4O4: C, 74.58; H, 8.87. Found: C, 74.61; H, 9.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365534B2
Source datasetuspto-grants-2016_06
ORD IDord-e7259cf2e5364460b60fa69f5dff678f
Source noteuspto-grants-2016_06