HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223540Generated: October 30, 2026
3,3,3-Trifluoropropanal → HCID 67298297, compound
https://huagongshe.com/reaction/2223540
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,3,3-Trifluoropropanal | HCID 68028 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Methyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetate | HCID 2734718 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67298297 | HCID 67298297 | — |
Reaction Steps
N-(Benzyloxycarbonyl)-α-phosphonoglycine trimethyl ester and DBU were dissolved in dry methylene chloride (50 mL) and the reaction mixture was chilled to −30° C. 3,3,3-Trifluoropropanal (1 eq) was added dropwise to the chilled and stirred solution and the reaction was allowed to stir for an additional hour at −30° C., and then overnight at ambient temperature. Methylene chloride (ca. 100 mL) was added and the organic phase was washed with 1N HCl (ca. 100 mL), then saturated brine (ca. 100 mL). The organic phase was dried over MgSO4, filtered, and concentrated by rotary evaporation. This crude product was purified by silica gel chromatography with a gradient of 10-30% ethyl acetate in hexanes to yield 2-benzyloxycarbonylamino-5,5,5-trifluoro-pent-2-enoic acid methyl ester as a white, crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07375134B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-463f7fbdb71541deb31f89d494ed45b4 |
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| Source note | uspto-grants-2008_05 |
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