HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535803Generated: October 26, 2026
Chloroacetaldehyde → (trans)-N-(2-chloroethyl)-2-(3'-(trifluoromethyl)biphenyl-4-yl)cyclopropanamine
https://huagongshe.com/reaction/535803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | (trans)-2-(3'-(Trifluoromethyl)biphenyl-4-yl)cyclopropanamine | HCID 66715451 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (trans)-N-(2-chloroethyl)-2-(3'-(trifluoromethyl)biphenyl-4-yl)cyclopropanamine | HCID 89123862 | 72.72% |
Reaction Steps
To a solution of (trans)-2-(3′-(trifluoromethyl)biphenyl-4-yl)cyclopropanamine (3.6 g, 38.26 mmol) in DCM (36 mL), 4° A molecular sieves was added followed by chloroacetaldehyde (5.8 mL, 38.26 mmol) and then stirred at RT for 1 h. After completion, monitored by TLC, cooled the reaction mixture at −10° C. and Na(CN)BH3 (2.88 g, 45.92 mmol) was added and stirred at RT for 2 h. After completion, the reaction mixture was quenched with NH4Cl (5%) and filtered through a pad of celite. The filtrate was extracted with DCM (2×50 mL), combined extracts were washed with water (40 mL), dried over anhydrous Na2SO4, filtered and evaporated. The residue was purified by flash column chromatography by using EtOAc: Pet ether to get (trans)-N-(2-chloroethyl)-2-(3′-(trifluoromethyl)biphenyl-4-yl)cyclopropanamine (3.2 g, 72.72%) as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859555B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f805dc976dbf40718e2982b836207687 |
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| Source note | uspto-grants-2014_10 |
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