HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoroanisole → 2-Fluoro-4-hydroxyphenylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoroanisole | HCID 67576 | — |
| Reactant | (3-Fluoro-4-methoxyphenyl)acetic acid | HCID 521176 | — |
| Product | 2-Fluoro-4-hydroxyphenylacetic acid | HCID 19361977 | — |
| Product | 2-(2-Fluoro-4-methoxyphenyl)acetic acid | HCID 19361978 | — |
Reaction Steps
The synthesis of 3-fluoro-4-methoxyphenylacetic acid 15 starting from 2-fluoroanisole has been described by M. Kucha{hacek over (r)} et al. (Collect. Czech. Chem. Commun. 1990, 55, 296-306). 2-Fluoro-4-methoxyphenylacetic acid 16 is obtained from 2-fluoro-4-hydroxyphenylacetic acid [S.-I. Sugita, S. Toda, T. Yoshiyasu, T. Teraji, Mol. Cryst. Liq. Cryst. 1993, 237, 399-406; E. J. Corey, J. P. Dittami, J. Am. Chem. Soc. 1985, 107, 256-257; H. H. Wassermann, J. Wang, J. Org. Chem. 1998, 63, 5581-5586] by dimethylation and ester saponification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08303844B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-b45b249f4bc7445ab95964ed4b493413 |
| Source note | uspto-grants-2012_11 |