HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-(4-t-Butylphenyl)propionyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(4-Tert-butylphenyl)propanoic acid | HCID 4962173 | — |
| Reactant | (5-Bromo-1,3-phenylene)bis(trimethylsilane) | HCID 12884904 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Catalyst | 3-(4-Tert-butylphenyl)propanoic acid | HCID 4962173 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-t-Butylphenyl)propionyl chloride | HCID 18402888 | 76.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479424B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-e680c120a49a438ba181fd2af4e3854c |
| Source note | uspto-grants-2002_11 |