Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429186Generated: November 2, 2026

Sulfuric Acid → (1-Hydroxymethyl-2-vinylcyclopropyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1429186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantEthyl 1-((tert-butoxycarbonyl)amino)-2-vinylcyclopropanecarboxylateHCID 22091725—
CatalystAmmoniummolybdate cerium sulfateHCID 131730262—
SolventTetrahydrofuranHCID 8028—
Product(1-Hydroxymethyl-2-vinylcyclopropyl)-carbamic acid tert-butyl esterHCID 6859181796%

Reaction Steps

To a solution of 1-tert-butoxycarbonylamino-2-vinyl-cyclopropanecarboxylic acid ethyl ester (0.51 g, 2.0 mmol) in THF (10 ml) at 0° C. was added a 2M solution of lithiumborohydride (4 ml, 8 mmol). The reaction mixture was monitored by TLC (7:3 hexane-ethyl acetate, stained using ammoniummolybdate-cerium sulfate in aq. 10% sulfuric acid) and after stirring overnight at rt, the reaction was carefully quenched using aq. 10% citric acid (25 ml, dropwise addition at 0° C.). The obtained mixture was washed with dichloromethane (3×10 ml), and the combined organic layers were dried (Na2SO4), filtered and concentrated. Flash chromatography of the residue using 1:1 hexane-ethyl acetate as eluent, followed by concentration of the appropriate fractions and drying the residue in vacuum overnight, gave the product as a colourless syrup (0.407 g, 1.91 mmol, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937080B2
Source datasetuspto-grants-2015_01
ORD IDord-4254e4682a6c4e83b9f1349423e2128f
Source noteuspto-grants-2015_01