HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799296Generated: October 30, 2026
Potassium Hydroxide → Tert-butyl (2s)-2-[(diphenylmethylene)amino]-3-[4-(trifluoromethoxy)phenyl]propanoate
https://huagongshe.com/reaction/1799296
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethoxy)benzene | HCID 142785 | — |
| Reactant | N-(Diphenylmethylene)glycine tert-butyl ester | HCID 688171 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl (2s)-2-[(diphenylmethylene)amino]-3-[4-(trifluoromethoxy)phenyl]propanoate | HCID 90973280 | 88% |
Reaction Steps
1-(Bromomethyl)-4-(trifluoromethoxy)benzene (28.1 g, 0.110 mol) and 50% potassium hydroxide (225 mL, 2.00 mol) were added to a toluene (1 L) suspension of tert-butyl [(diphenylmethylene)amino]acetate (29.5 g, 0.10 mol) and N-(9-anthracenylmethyl)cinchonidinium chloride (5.79 g, 0.01 mol) under ice-cooling with stirring. The mixture was vigorously stirred at the same temperature for 3.25 hours and then separated into an organic layer and an aqueous layer. The aqueous layer was extracted with ethyl acetate (200 mL), and the organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate, 20:1, 15:1, and 10:1, V/V) to give 41.2 g of the title compound (mixture of a yellow oil and a yellow solid, yield: 88%, optical purity: 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344029B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ae47d7660b0243dcae19fec997736c8d |
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| Source note | uspto-grants-2013_01 |
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