HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598708Generated: October 28, 2026
Triethylamine → N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide
https://huagongshe.com/reaction/598708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-tert-Butyl-2,6-diaminoanisole | HCID 4177235 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide | HCID 10214710 | 87.1% |
Reaction Steps
To an oven dried 250 mL round bottom flask containing 5.0 g (25.73 mmol) 5-tert-butyl-2-methoxy-benzene-1,3-diamine, 150 mL DCM was added. The reaction mixture was cooled to 0° C. after which triethylamine (5.0 mL, 36.0 mmol) was added followed by the drop wise addition of methylsulfonyl chloride (1.99 mL, 25.7 mmol). The reaction was allowed to stir at 0° C. for 30 min. then warmed to room temperature stirring for an additional 2 h. The reaction mixture was poured over saturated solution of sodium bicarbonate (100 mL) and the layers separated. The aqueous layer was washed twice more with 50 mL dichloromethane and the combined organic layers were dried over magnesium sulfate and concentrated under vacuum to afford a crude oil that was purified by flash chromatography (silica gel, 1:1 EtOAc:Hex) to yield 6.1 g of the desired product (87%). Calculated mass=272. Observed mass=273
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897599B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-a4059456a0cb40a6946a821105f41241 |
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| Source note | uspto-grants-2011_03 |
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