HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 20475695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 54057565 | HCID 54057565 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20475695 | HCID 20475695 | — |
Reaction Steps
Sodium hydride dispersion (55-60%, 2 mmol) was further dispersed in benzene (4 ml) and added gradually to a solution of diethyl (5-chloropyrimidin-2-sulfonyl)methanephosphonate (0.66 g, 2 mmol) in benzene (4 ml). The mixture was stirred for 10 min before a solution of benzaldehyde (0.21 g, 2 mmol) in benzene (2 ml) was added. The resultant mixture was stirred at room temperature overnight before extraction with water. Evaporation of the dried (MgSO4) benzene solution left the product which was recrystallised from ethanol; yield 0.20 g 35%, m.p. 150° C. 1H NMR (CDCl3): δ7.24 and 7.90 (2H-vinyl, Jvic 16 Hz), 7.60 (Ph, m.), 8.90 (2H-4,6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423047 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-41b89d508c264a3081fcd6a97f634d60 |
| Source note | uspto-grants-1983_12 |