HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Fluorobenzaldehyde → 2-(Ethylsulfanyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | 2-(Isopropylthio)benzaldehyde | HCID 11206137 | — |
| Product | 2-(Ethylsulfanyl)benzaldehyde | HCID 13082726 | 78% |
Reaction Steps
114A (10.4 g, 78% yield) was prepared from 2-fluorobezaldehyde (10 g, 81 mmol) and thioethane (5.5 g, 89 mmol) using a procedure similar to that used in the preparation of 11A. 1H NMR (400 MHz, Methanol-d4) δ ppm 1.23-1.42 (m, 3H) 2.98 (q, J=7.34 Hz, 2H) 7.17-7.37 (m, 1H) 7.38-7.64 (m, 2H) 7.81 (dd, J=7.70, 1.59 Hz, 1H) 10.30 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07622585B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-2e00be5c901147ababb9c93327081b03 |
| Source note | uspto-grants-2009_11 |