HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568878Generated: October 31, 2026
Sodium Bicarbonate → HCID 53794764, compound
https://huagongshe.com/reaction/568878
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,5-Dibenzyloxybenzaldehyde | HCID 561351 | — |
| Reactant | Phosphonium, [3-(1-methoxy-1-methylethoxy)propyl]triphenyl-, bromide | HCID 10950828 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53794764 | HCID 53794764 | 58.4% |
Reaction Steps
A stirred suspension of [3-(1-methoxy-1-methylethoxy)propyl](triphenylphosphonium)bromide (4 g) in dry THF (25 ml) at 0° C. was heated with butyl lithium (5.28 ml) and the mixture stirred at 0° C. for 10 min. 3,5-Bis(phenylmethoxy)benzaldehyde (2.24 g) in dry THF (15 ml) was added and the mixture stirred for a further 45 min at room temperature under nitrogen, diluted with ER (100 ml) and filtered through silica (20 g) twice. The filtrate was evaporated in vacuo to give a yellow oil which was dissolved in a mixture of THF (50 ml), water (5 ml) and 2M hydrochloric acid (1 ml) and left at room temperature for 30 min. The mixture was basified with sodium bicarbonate solution and extracted with ER (200 ml). The organic phase was washed with water (150 ml), brine (100 ml), dried and evaporated in vacuo to give a yellow oil. Purification by FCC eluting with ER-CX (3:2) gave a colourless oil (1.48 g). T.l.c. (ER-CX 3:1) Rf 0.26
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04730008 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-004c6c7d24d5455488fd82eeb388077e |
|---|
| Source note | uspto-grants-1988_03 |
|---|