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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017146Generated: October 31, 2026

Thionyl Chloride → 3-(4-t-Butylphenyl)propionyl chloride

https://huagongshe.com/reaction/1017146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(4-Tert-butylphenyl)propanoic acidHCID 4962173—
Reactant(5-Bromo-1,3-phenylene)bis(trimethylsilane)HCID 12884904—
CatalystDimethylformamideHCID 6228—
Catalyst3-(4-Tert-butylphenyl)propanoic acidHCID 4962173—
SolventDichloromethaneHCID 6344—
Product3-(4-t-Butylphenyl)propionyl chlorideHCID 1840288876.5%

Reaction Steps

A 2 L 3 neck round bottom flask fit with a condenser, thermometer, nitrogen inlet, and overhead stirrer was charged with 3-(4-t-butylphenyl)propionic acid (118.7 g, 0.576 mol),thionyl chloride (210 mL, 2.88 mol), dimethylformamide (3 drops), and methylene chloride solvent. The reaction was refluxed for 3 hours and additional 3-(4-t-butylphenyl)propionic acid (8.17 g, 0.040 mol) was added to the reactor and refluxed for an additional hour. After allowing to stand overnight, the reaction was stripped of volatiles to yield the crude 3-(4-t-butylphenyl)propionyl chloride (99.0 g). 1HNMR (CDCl3, 500 MHz) δ7.33 (d, JAB=8 Hz, 2H); 7.12 (d, JAB=8 Hz, 2H); 3.20 (t, J=7.5 Hz, 2H); 2.98 (t, J=7.5, 2H); 1.31 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479424B1
Source datasetuspto-grants-2002_11
ORD IDord-e680c120a49a438ba181fd2af4e3854c
Source noteuspto-grants-2002_11