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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815120Generated: October 30, 2026

Iodobenzene → HCID 16074360, compound

https://huagongshe.com/reaction/1815120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
Reactant3-IodophenolHCID 12272—
ReactantHCID 16074350HCID 16074350—
ReactantHCID 22499801HCID 22499801—
ProductHCID 16074360HCID 16074360—

Reaction Steps

The title compound was prepared analogously to Example 6, except 3-iodophenol was used for iodobenzene, and 6-but-3-ynyl-6-cyclopentyl-4-ethoxy-5,6-dihydro-pyran-2-one, described in Step 2 of that example, was used for 6-but-3-ynyl-6-cyclopentyl-dihydro-pyran-2,4-dione. 1H NMR (CDCl3): δ 1.26 (t, 2H, J=7.16 Hz), δ 1.51-1.81 (m, 8H), δ 2.10 (t, 2H, J=7.54 Hz), δ 2.36 (t, 1H, J=8.10 Hz), δ 2.48 (d, 1H, J=17.71 H), δ 2.52 (t, 2H, J=7.35 Hz), δ 2.68 (d, 1H, J=17.52 Hz), δ 3.94 (q, 2H, J=7.35 Hz), δ 5.14 (d, 2H, J=6.22 Hz), δ 6.77 (dd, 1H, J=5.65 Hz, J=2.45 Hz), δ 6.87 (s, 1H), δ 6.95 (d, 1H, J=6.59 Hz), δ 7.14 (t, 1H, J=7.91 Hz). Anal. Calcd. For C22H26O4 0.3 EtOAc: C, 73.16, H 7.52. Found: C, 73.18, H, 7.57; ESIMS (M+Na+) 377.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878727B2
Source datasetuspto-grants-2005_04
ORD IDord-408e7820b7d045318a42be33d35a3915
Source noteuspto-grants-2005_04