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 | US05414007 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-8c1f96e09b15442f8db49c86ece5b4d6 |
| Source note | uspto-grants-1995_05 |