HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 712035Erstellt: 26. Oktober 2026
Triethylamine → tert-butyl N-[3-(hydroxymethyl)cyclohexyl]carbamate
https://huagongshe.com/reaction/712035
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 3-(((Tert-butoxy)carbonyl)amino)cyclohexane-1-carboxylic acid | HCID 4420316 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | tert-butyl N-[3-(hydroxymethyl)cyclohexyl]carbamate | HCID 22106830 | 92% |
Reaktionsschritte
To a mixture of 3-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid (from Alfa Aesar, 3.3 g, 14 mmol) and triethylamine (3.8 mL, 27 mmol) in tetrahydrofuran (40 mL) at 0° C. was added dropwise ethyl chloroformate (1.9 mL, 20 mmol). The mixture was stirred at 0° C. for 10 min and then at room temperature for 20 min. The mixture was filtered to remove the white solid and then cooled to 0° C. A mixture of sodium tetrahydroborate (1.0 g, 27 mmol) and methanol (1 mL) was added slowly. The mixture was stirred at room temperature for 1 h. The mixture was quenched with 1N aq. HCl solution and extracted with EtOAc. The extracts were concentrated and purified on silica gel column (eluting with 75% EtOAc in hexanes) to give the desired product (2.88 g, 92%). LCMS calculated for C13H23NO3Na (M+Na)+: m/z=252.2. Found: 252.1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09181271B2 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-7ebf58bd530c4075a2707355eef48acc |
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| Quellennotiz | uspto-grants-2015_11 |
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