HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690704Generated: November 1, 2026
4-Butylphenylboronic acid → HCID 16047072, compound
https://huagongshe.com/reaction/1690704
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Butylphenylboronic acid | HCID 4100860 | — |
| Reactant | 5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-2-carboxylic acid | HCID 66904833 | — |
| Reactant | HCID 66904900 | HCID 66904900 | — |
| Product | HCID 16047072 | HCID 16047072 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153671B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-649b0ee705cd4e7eae280dfb3a63947f |
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| Source note | uspto-grants-2012_04 |
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