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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36357Generated: October 25, 2026

4-tert-Butylphenylacetylene → 4-(1,1,4-Trimethylpentyl)phenylethyne

https://huagongshe.com/reaction/36357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenylacetyleneHCID 2757302—
ReactantTrimethylsilyl[4-(1,1,4-trimethylpentyl)]phenylethyneHCID 14989666—
Product4-(1,1,4-Trimethylpentyl)phenylethyneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05414007
Source datasetuspto-grants-1995_05
ORD IDord-8c1f96e09b15442f8db49c86ece5b4d6
Source noteuspto-grants-1995_05