HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 7-(Methylsulfanyl)-2-naphthoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-Bromo-7-(methylsulfanyl)naphthalene | HCID 44550985 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(Methylsulfanyl)-2-naphthoic acid | HCID 44550986 | 79% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A stirred solution of 199 (850 mg, 3.36 mmol) in THF (10 mL) was treated at −78° C. with n-BuLi (2.5 M in hexanes, 1.48 mL, 3.70 mmol) under N2. The mixture was stirred at −78° C. for 15 nm in, then treated with excess CO2(g) and allowed to warm to room temperature. The solvent was removed under reduced pressure, and the residue was partitioned between water and EtOAc. The aqueous layer was acidified, and the resulting solid was crystallised from MeOH to give 7-(methylsulfanyl)-2-naphthoic acid (200) (577 mg, 79%): mp 217° C.; 1H NMR [(CD3)2SO] δ 13.0 (v br, 1H), 8.53 (d, J=0.7 Hz, 1H), 7.98-7.87 (m, 4H), 7.53 (dd, J=8.7, 1.9 Hz, 1H), 2.60 (s, 3H). Anal. (C12H10O2S) C, H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07718688B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-42b668baebf54e05b98cef3999cb7c98 |
| Source note | uspto-grants-2010_05 |