HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 22323720, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Butanoic acid, 3-[(4-methoxyphenyl)thio]-3-methyl- | HCID 10171427 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 22323720 | HCID 22323720 | — |
Reaction Steps
To a solution of 3-(4-methoxy-pbenylsulfanyl)-3methyl-butyric acid (20.0 g. 83.2 mmol) in 250 mL of benzene at room temperature was added a solution of oxalyl chloride (15.84 g. 124.8 mmol) in 10 mi of benzene over 30 minutes. After 4 h, the solution was washed with ice cold 5% aqueous NaOH (CAUTION: a large volume of gas is released during this procedure) followed by ice cold H2O, and finally saturated aqueous NaCl. The solution was dried (Na2SO4) and concentrated under reduced pressure to give a clear yellow oil. This material (3(4-methoxy-phenylsulfanyl)3-methyl-butyroyl chloride) was used without further purification in the next step. 1H NMR (300 MHz, CDCl3) δ: 7.45 (2H, d, J=8.8 Hz), 3.84 (3H, s), 3.12 (2H, s, 1.41 (6H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218128B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-89cebc36228a49b1abaefd9b50ac60b5 |
| Source note | uspto-grants-2001_04 |