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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690704Generated: November 1, 2026

4-Butylphenylboronic acid → HCID 16047072, compound

https://huagongshe.com/reaction/1690704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Butylphenylboronic acidHCID 4100860—
Reactant5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-2-carboxylic acidHCID 66904833—
ReactantHCID 66904900HCID 66904900—
ProductHCID 16047072HCID 1604707234%

Reaction Steps

The title material is prepared in 34% yield by reacting 5-Oxo-6,7,8,9-tetrahydro-5H-benzocycloheptene-2-carboxylic acid (J. Org. Chem. 1962, 27(1), p 70-76) and (4′-Butyl-2-fluoro-biphenyl-3-yl)-hydrazine hydrochloride (prepared as in example 69, steps 1 and 2 except using 4-n-butylphenylboronic acid as the coupling partner) in an analogous manner to example 1, step 3 except that purification is accomplished by reverse phase mass triggered HPLC: 1H NMR (Acetone-d6) δ 10.72 (bs, 1H), 8.09 (d, 1H), 7.99 (d, 1H), 7.92 (s, 1H), 7.58 (d, 2H), 7.45 (d, 1H), 7.31 (d, 2H), 7.17 (dd, 1H), 3.18 (t, 2H), 3.10-3.04 (m, 2H), 2.72 (t, 2H), 2.22-2.14 (m, 2H), 1.73-1.64 (m, 2H), 1.45-1.38 (m, 2H), 0.96 (t, 3H); LC/MS calculated for [M+H]+ C28H26FNO2: 428.2, found: 428.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153671B2
Source datasetuspto-grants-2012_04
ORD IDord-649b0ee705cd4e7eae280dfb3a63947f
Source noteuspto-grants-2012_04