HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 6-Methoxy-1-naphthoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Methoxy-1-naphthoic acid | HCID 4413708 | — |
| Product | 6-Methoxy-1-naphthoyl chloride | HCID 57516693 | — |
Reaction Steps
Under an argon atmosphere, 6-methoxy-1-naphthoic acid (synthesized by the process of J. D. Moseley and J. P. Gilday, Tetrahedron, 62, 4690-4697 (2006)) (1.20 g, 5.93 mmol) was dissolved in thionyl chloride (5.00 mL, 68.8 mmol) and the solution was heated to reflux for 3 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure to give the crude product of 6-methoxy-1-naphthoyl chloride (22) as a colorless oil. The product was used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056840B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-5b5c998e3cfe4944a7b5e5a414fe4c8a |
| Source note | uspto-grants-2015_06 |