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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822431Generated: November 3, 2026

tert-Butyl carbazate → tert-butyl N-[(E)-hept-6-enylideneamino]carbamate

https://huagongshe.com/reaction/1822431

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbazateHCID 70091—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-HeptenalHCID 5283320—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Producttert-butyl N-[(E)-hept-6-enylideneamino]carbamateHCID 8744439761.6%

Reaction Steps

To a solution of 5 (68 mg, 0.610 mmol) and tert-butyl carbazate (81 mg, 0.613 mmol) in MeOH (5 mL) was added ground molecular sieves (115 mg, 3 Å). The mixture was stirred for 3 h after which it was filtered through celite and evaporated. The residue was dissolved in dry THF (3 mL) and AcOH (3 mL). NaBH3CN (95 mg, 1.51 mmol) was added and the solution was stirred over night. The reaction mixture was diluted with saturated NaHCO3 solution (6 mL) and EtOAc (6 mL). The organic phase was washed with brine, saturated NaHCO3, brine, dried over MgSO4 and evaporated. The cyanoborane adduct was hydrolyzed by treatment with MeOH (3 mL) and 2 M NaOH (1.9 mL). The mixture was stirred for 2 h and the MeOH was evaporated. H2O (5 mL) and DCM (5 mL) were added and the water phase was extracted three times with DCM. The combined organic phases were dried and evaporated. Purification by flash column chromatography (toluene/ethyl acetate 9:1 with 1% triethylamine and toluene/ethyl acetate 6:1 with 1% triethylamine) provided the title compound (85 mg, 61%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608590B2
Source datasetuspto-grants-2009_10
ORD IDord-895219dfae5a47c68b89c5f359423b1a
Source noteuspto-grants-2009_10