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HRID 712035Erstellt: 26. Oktober 2026

Triethylamine → tert-butyl N-[3-(hydroxymethyl)cyclohexyl]carbamate

https://huagongshe.com/reaction/712035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
EduktSodium borohydrideHCID 4311764—
Edukt3-(((Tert-butoxy)carbonyl)amino)cyclohexane-1-carboxylic acidHCID 4420316—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl N-[3-(hydroxymethyl)cyclohexyl]carbamateHCID 2210683092%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181271B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-7ebf58bd530c4075a2707355eef48acc
Quellennotizuspto-grants-2015_11