HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556726Generated: October 31, 2026
Water → 2-(3,4-Dimethoxyphenyl)ethyl 2,2,2-trichloroethanimidate
https://huagongshe.com/reaction/556726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,4-Dimethoxyphenethyl alcohol | HCID 81911 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3,4-Dimethoxyphenyl)ethyl 2,2,2-trichloroethanimidate | HCID 16743807 | 95% |
Reaction Steps
A 500 mL 2-necked round bottom flask equipped with an argon inlet, rubber septum and magnetic stir bar was charged with NaH (80% dispersion, 5.2 g, 173.3 mmol). NaH was washed with anhydrous hexanes (15 mL) prior to the addition of 50 mL of anhydrous CH2Cl2 and of 3,4-dimethoxyphenethyl alcohol (20.0 g, 109.8 mmol) in anhydrous CH2Cl2 (30 mL). The solution was allowed to stir at r.t. for 75 min. The solution was then cooled to 0° C. prior to the dropwise addition of trichloroacetonitrile (16.5 mL, 23.8 g, 164.7 mmol) at 0° C. The solution was stirred for 15 min at 0° C. and 2 hr at room temperature. Distilled water (150 mL) was slowly added dropwise to quench the reaction. The aqueous layer was then extracted with CH2Cl2 (4×100 mL). The combined organic extracts were washed with brine (100 mL), dried over anhydrous MgSO4 and concentrated by rotary evaporation to afford a brown syrup (26.8 g, 95%). The product was allowed to solidify overnight at −20° C. Rf 0.74 (EtOAc-hexanes, 1:2, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058304B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-a03cb1a910d9497a9e778ff5e0321b65 |
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| Source note | uspto-grants-2011_11 |
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