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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424934Generated: October 26, 2026

Ethyl Acetate → (R)-Tert-butyl 2-methylazetidine-1-carboxylate

https://huagongshe.com/reaction/424934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithiumtriethylborohydrideHCID 23664628—
Reactanttert-Butyl (S)-2-(((methylsulfonyl)oxy)methyl)azetidine-1-carboxylateHCID 59371380—
SolventTetrahydrofuranHCID 8028—
Product(R)-Tert-butyl 2-methylazetidine-1-carboxylateHCID 5778471730%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(S)-Methanesulfonyloxymethyl-azetidine-1-carboxylic acid tert-butyl ester was (4.83 g, 18.2 mmol) was taken up in THF (11 mL), cooled to 0° C. under N2, treated drop-wise with a lithium triethylborohydride (1.0 M in THF, 73 mL), stirred at ambient temperature for 6 hours, treated with ethyl acetate (500 mL), washed with water, washed with 0.25 M HCl, washed with NaHCO3 solution, washed with brine (2×), dried (MgSO4), filtered, concentrated and purified by chromatography on silica gel eluting with a gradient of 10:1 and then 5:1 hexane:ethyl acetate to provide 0.95 g (30%) of the title compound. 1H NMR (300 MHz, CDCl3) δ 1.37 (d, J=6.10 Hz, 3 H) 1.44 (s, 9 H) 1.76 (m, 1 H) 2.27 (m, 1 H) 3.81 (t, J=7.46 Hz, 2 H) 4.28 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106088B2
Source datasetuspto-grants-2012_01
ORD IDord-696fda201cc14cc5ab920bb930302a31
Source noteuspto-grants-2012_01