HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987146Generated: October 30, 2026
1,1,3,3-Tetramethylguanidine → Ethyl 3-[4-(benzyloxy)phenyl]-2-ethoxyprop-2-enoate
https://huagongshe.com/reaction/987146
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | — |
| Reactant | Phosphonium, (1,2-diethoxy-2-oxoethyl)triphenyl-, chloride (1:1) | HCID 11327835 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 3-[4-(benzyloxy)phenyl]-2-ethoxyprop-2-enoate | HCID 54423854 | 85.7% |
Reaction Steps
Tetramethylguanidine (42.3 g; 0.37 mole) was slowly added to a solution of 4-benzyloxybenzaldehyde (75.6 g; 0.36 mole) and (1,2-diethoxy-2-oxoethyl) (triphenyl)phosphonium chloride (130.7 g; 0.304 mole) dissolved in chloroform (800 ml) at 0° C. After stirring at room temperature over night, the solvent was evaporated in vacuo. The residue was dissolved in diethyl ether, insoluble material was filtered off and the filtrate was washed with sodium bicarbonate and dried (magnesium sulfate). The procedure was repeated once and thereafter the crude product was stirred overnight with a sodium bisulfite saturated water solution. The solid material was filtered off, the product was extracted with diethyl ether, dried (magnesium sulfate) and the solvent was evaporated in vacuo to give 85 g (yield 73%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630509B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-a440e18e326f42cc9050eebfa1720eaf |
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| Source note | uspto-grants-2003_10 |
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