HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838993Generated: October 30, 2026
Potassium Hydroxide → 4-{[(2,2-Dichlorocyclopropyl)methyl]sulfanyl}-2-nitroaniline
https://huagongshe.com/reaction/838993
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Amino-3-nitrophenyl thiocyanate | HCID 104677 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-BROMOMETHYL-1 1-DICHLOROCYCLOPROPANE | HCID 4739582 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-{[(2,2-Dichlorocyclopropyl)methyl]sulfanyl}-2-nitroaniline | HCID 20532839 | 54.6% |
Reaction Steps
To a stirred mixture of 11.75 g (0.06 mole) of 2-nitro-4-thiocyanoaniline in 500 ml of absolute ethanol under N2 there is added 2.5 g (0.06 mole) of sodium borohydride in portions. The mixture is stirred at room temperature for 15 minutes and then refluxed for 15 minutes. The heating mantle is removed and 3.9 g (0.06 mole) of KOH in 30 ml of absolute ethanol is added. The mixture is stirred for 1 minute. A solution of 12.25 g (0.06 mole) of 1-bromomethyl-2,2-dichlorocyclopropane in 30 ml of absolute ethanol is added and the mixture is stirred at room temperature for 15 minutes and then refluxed for 2 hours. Equal amounts of H2O and CHCl3 are added until 2 layers are formed. The organic layer is separated, dried (MgSO4), and the solvent removed in vacuo to give a red oil which is chromatographed on silica gel. Elution with ethyl ether gives 9.6 g of red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093732 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-cba037499cf64fc2a329aaaa220dee3b |
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| Source note | uspto-grants-1978_06 |
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