HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylphenylacetylene → 4-(4-Methylpentyl)-phenylethyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylphenylacetylene | HCID 2757302 | — |
| Reactant | Trimethylsilyl[4-(4-methylpentyl)]phenylethyne | HCID 54327813 | — |
| Product | 4-(4-Methylpentyl)-phenylethyne | HCID 15337560 | — |
Reaction Steps
Using the same general procedure as described for Compound 19), but using instead trimethylsilyl [4-(4-methylpentyl)] phenylethyne (Compound 31), the title compound was synthesized as a colorless oil. PMR (CDCl3) & 0.94 (6H, d, J~6.6 Hz), 1.20-1.32 (2H, m), 1.56-1.62 (3H, m), 2.64 (2H, t, J 7.8 Hz), 3.08 (1H, s), 7.18 (2H, d, J 8.1 Hz), 7.47 (2H, d, J~8.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05175185 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-5c931baf794c4af2bf1056a0ed8fc1de |
| Source note | uspto-grants-1992_12 |