HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423087Generated: October 31, 2026
Ethanol → tert-butyl N-[2-amino-1-(4-chlorophenyl)ethyl]carbamate
https://huagongshe.com/reaction/423087
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-(Tert-butoxycarbonylamino)-2-(4-chlorophenyl)ethyl methanesulfonate | HCID 57750278 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-butyl N-[2-amino-1-(4-chlorophenyl)ethyl]carbamate | HCID 57750386 | 99% |
Reaction Steps
A solution of 2-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)ethyl methanesulfonate (Intermediate 23) (535 mg, 1.53 mmol) in DMF (8 mL) was treated with sodium azide (199 mg, 3.06 mmol) and the mixture was heated at 80° C. for 1 hour. The mixture was cooled and allowed to stir at room temperature overnight. The solution was partitioned between ethyl acetate and water. The organic layer was washed twice with water then dried with magnesium sulfate, filtered and concentrated until the final volume was approximately 5 mL. Ethanol (20 mL) and 10% palladium on carbon (75 mg, 0.07 mmol) were added. The resulting suspension was stirred under an atmosphere of hydrogen at ambient pressure and temperature for 1 hour. The mixture was filtered and the filtrate was concentrated under reduced pressure to give tert-butyl 2-amino-1-(4-chlorophenyl)ethylcarbamate as a gum (410 mg, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101623B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-32c5a0e8da454e40985b831be5d49397 |
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| Source note | uspto-grants-2012_01 |
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