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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409468Generated: October 30, 2026

Hydrochloric Acid → HCID 86648402, compound

https://huagongshe.com/reaction/409468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantHexaneHCID 8058—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant((R)-2-cyano-1-ethyl-ethyl)-carbamic acid tert-butyl esterHCID 10285865—
ProductHCID 86648402HCID 86648402—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of ((R)-2-cyano-1-ethyl-ethyl)-carbamic acid tert-butyl ester (10 mmol; 1.98 g) in Et2O (50 mL) is slowly added a 0.97 M n-hexane solution (40 mmol; 41 mL) of DIBAL under nitrogen at −78° C. The reaction mixture is warmed to −40° C. and stirred for an additional 3.5 hours. Another 1.00 M n-hexane solution (30 mmol; 30 mL) of DIBAL is added to the suspension at the same temperature. After stirring for additional 1.5 hours, the solution is quenched by careful addition of 1 ml of MeOH then immediately poured into 25 ml of saturated aqueous ammonium chloride solution in a separatory funnel. Shake mixture and leave until it reaches room temperature. Aqueous 1M HCl is added to reach a pH of 3-4. The solution is extracted three times with EtOAc and the combined organic layer is washed with an aqueous 1M HCl/brine (1:1) solution and twice with a saturated aqueous NaHCO3/brine (1:1) solution, dried over Na2SO4, filtered and concentrated under reduced pressure and purified by column chromatography on silica gel (eluent; n-hexane/EtOAc) to give ((R)-1-ethyl-3-oxo-propyl)-carbamic acid tent-butyl ester (590 mg, 29%); ESI-MS m/z: 146 [M+−tBu+2], Retention time 2.17 min (condition A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759365B2
Source datasetuspto-grants-2014_06
ORD IDord-f117289299e74971bb6428da1be57323
Source noteuspto-grants-2014_06