HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587926Generated: November 3, 2026
Dimethyl Sulfate → Ethyl 4-(2-(tert-butoxycarbonyl(methyl)amino)ethyl)benzoate
https://huagongshe.com/reaction/587926
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | Ethyl 4-(2-(tert-butoxycarbonylamino)ethyl)benzoate | HCID 67360059 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-(2-(tert-butoxycarbonyl(methyl)amino)ethyl)benzoate | HCID 68475038 | — |
Reaction Steps
To a solution of 1.25 g (4.26 mmol) of ethyl 4-(2-(tert-butoxycarbonylamino)ethyl)benzoate in 40 mL of dry THF under a nitrogen atmosphere was added dropwise, 4.7 mL (4.7 mmol) of NaHMDS (1.0 M in THF) at 0° C. After stirring for 10 min, 0.50 mL (5.3 mmol) of dimethyl sulfate was added and the reaction was warmed to 22° C. and stirred for about 16 h. The reaction was quenched by adding 25 mL of saturated NaHCO3 and the mixture was extracted with DCM (2×25 mL). The combined organic extracts were dried (Na2SO4) and evaporated and the residue was purified by flash chromatography on silica gel, eluting first with hexane and then gradually increasing to 10% ethyl acetate/hexane to give ethyl 4-(2-(tert-butoxycarbonyl(methyl)amino)ethyl)benzoate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227918B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-6408d5a3ec394cee8bc733ed94daa33e |
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| Source note | uspto-grants-2016_01 |
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