HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501881Generated: October 25, 2026
Tert-Butyl hypochlorite → 2-[(4,6-Dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline
https://huagongshe.com/reaction/501881
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-(Methoxymethyl)aniline | HCID 12334306 | — |
| Reactant | 2-Methylthiomethyl-4,6-dimethoxypyrimidine | HCID 57428123 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(4,6-Dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline | HCID 16726314 | 58.8% |
Reaction Steps
2-Methoxymethylaniline (0.68 g, 4.96 mmol) was dissolved in dichloromethane (50 ml) and the solution was cooled to −70° C. To the cooled solution a solution of tert-butyl hypochlorite (0.54 g, 4.96 mmol) in dichloromethane (1 ml) was added dropwise and the solution was stirred at −70° C. for 10 minutes. To the obtained reaction solution a solution of 2-methylthiomethyl-4,6-dimethoxypyrimidine (0.893 g, 4.46 mmol) in dichloromethane (5 ml) was added dropwise and the solution was stirred at −70° C. for 30 minutes. To the obtained reaction solution a 28% methanol solution of sodium methoxide (4 ml) was added and the solution was stirred until its temperature reached room temperature. Water was added to the reaction solution and the organic layer was separated. The water layer was further extracted twice with dichloromethane. The organic layer was washed with water and dried. Then dichloromethane was distilled off under reduced pressure and the obtained oily substance was purified by column chromatography using 1:6 mixed solvent of ethyl acetate and hexane as eluent to obtain 2-[(4,6-dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline (0.88 g, yield 53%) as oily substance;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772395B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-8f4ca55198c64fdfb6527531970c3dc7 |
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| Source note | uspto-grants-2010_08 |
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