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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549269Generated: October 30, 2026

2-tert-butylbenzenethiol → HCID 67157078, compound

https://huagongshe.com/reaction/549269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-butylbenzenethiolHCID 2795032—
ReactantHCID 60069826HCID 60069826—
CatalystHCID 178418397HCID 178418397—
Solvent1-ButanolHCID 263—
ProductHCID 67157078HCID 6715707871%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-(7-bromo-isoquinoline-1-yl)-piperazine-1-carboxylic acid, tert-butyl ester (0.5 g, 1.3 mmol), 2-t-butyl-thiophenol (0.216 g, 1.3 mmol), Nat-BuO (0.44 g, 4.5 mmol), Pd(PPh3)4 (74 mg, 0.065 mmol) in n-BuOH (10 mL) was heated at 110° C., 3 h. The reaction mixture was filtered. The filtrate was concentrated and the residue was dissolved in ethyl acetate. The organic phase was washed with water (50 mL×3), separated and dried (MgSO4), filtered. The volatiles were evaporated and the residue was purified by flash column chromatography (SiO2, n-heptane: ethyl acetate 8:2) to give 440 mg of the title compound as colorless oil (yield 71%). 1H NMR (CDCl3) δ 8.00-8.10 (m, 2H), 7.15-7.65 (m, 7H), 3.60-3.70 (m, 1H), 3.30-3.45 (m, 4H), 3.05-3.20 (m, 3H), 1.55 (s, 9H), 1.50 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943639B2
Source datasetuspto-grants-2011_05
ORD IDord-26bec4d342624a6f88af1dc60869fdb1
Source noteuspto-grants-2011_05