HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylphenylacetylene → 4-(1,1,4-Trimethylpentyl)phenylethyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylphenylacetylene | HCID 2757302 | — |
| Reactant | Trimethylsilyl[4-(1,1,4-trimethylpentyl)]phenylethyne | HCID 14989666 | — |
| Product | 4-(1,1,4-Trimethylpentyl)phenylethyne | HCID 14989668 | — |
Reaction Steps
Using the same general procedure as described for Compound 19, but using instead trimethylsilyl[4-(1,1,4-trimethylpentyl)]phenylethyne (Compound 34), the title compound was synthesized as a colorless oil. PMR (CDCl3): & 0.81 (6H, d, J-6.6 Hz), 0.85-0.96 (2H, m), 1.29 (6H, s), 1.32-1.48 (1H, m). 1.55-1.66 (2H, m)., 3.04 (1H, s), 7.29 (2H, d, J-8.4 Hz), 7.44 (2H, d, J-8.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516904 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-3667c4789d304e80a80032f866ed7b62 |
| Source note | uspto-grants-1996_05 |