HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091305Generated: October 31, 2026
1,1-Dichloroethane → HCID 66592460, compound
https://huagongshe.com/reaction/1091305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-Fluoro-2-methylpropan-2-amine hydrochloride | HCID 13935251 | — |
| Reactant | Benzyl Bis(2-oxoethyl)carbamate | HCID 15009275 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 66592460 | HCID 66592460 | 40% |
Reaction Steps
Bis-(2-oxoethyl)carbamic acid benzyl ester (0.81 g, 3.45 mmol) and 1,1-dimethyl-2-fluoroethylamine hydrochloride (0.40 g, 3.14 mmol) were dissolved dichloroethane (50 mL), and sodium triacetoxyborohydride (1.99 g, 9.41 mmol) was added thereto. The mixture was stirred for three days at room temperature. A saturated aqueous solution of sodium hydrogen carbonate (20 mL) was added to the reaction liquor, and the mixture was stirred for 30 minutes, and then extracted with methylenechloride. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and then the solvent was concentrated under reduced pressure. The obtained residue was purified by flash chromatography (Flash Chromatography System from Biotage AB, column size: 40S, n-hexane/ethyl acetate=1/1 to ethyl acetate), to obtain the title compound (370 mg, 29%), partially including impurities, as an oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129366B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-9db10dbdb57a4f0cbb6198c1d3ebaec6 |
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| Source note | uspto-grants-2012_03 |
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