HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74117Generated: October 27, 2026
Dimethyl Sulfate → (R)-N-benzyl-2-(ethoxycarbonylamino)-3-methoxypropionamide
https://huagongshe.com/reaction/74117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (R)-N-benzyl-2-(ethoxycarbonylamino)-3-hydroxypropionamide | HCID 53344986 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-N-benzyl-2-(ethoxycarbonylamino)-3-methoxypropionamide | HCID 53344987 | 70.96% |
Reaction Steps
To a 500 mL three-neck round bottom flask, 7.2 g (0.027 mol) (R)-N-benzyl-2-(ethoxycarbonylamino)-3-hydroxypropionamide, 300 mL ethyl acetate, 27.2 g (0.216 mol) dimethyl sulfate, and 2.0 g tetrabutylammonium bromide were added in sequence. At a normal temperature, 24.8 g 50% potassium hydroxide (0.2214 mol) solution was added. After the reaction was completed, 100 mL water was added, and the mixture was stirred for several minutes, and stood for layering. An organic layer was separated, and washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was evaporated, to obtain a transparent oily substance, which was triturated with n-hexane, suction-filtered, washed, and dried, to obtain a white solid of 5.37 g (0.01916 mol). The molar yield was 70.96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829226B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-97cd46039495446584bca2082a5cf2de |
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| Source note | uspto-grants-2014_09 |
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