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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421997Generated: October 29, 2026

Bromoacetonitrile → HCID 67243918, compound

https://huagongshe.com/reaction/2421997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67243918HCID 6724391842%

Reaction Steps

NaH (60% dispersion in mineral oil, 276 mg, 6.89 mmol) was added to an ice cold solution of tert-butyl 3-hydroxyazetidine-1-carboxylate (0.92 mg, 5.30 mmol) in THF (8 mL) and stirred for 15 mins. Bromoacetonitrile (0.52 mL, 7.43 mmol) was added dropwise and the reaction mixture allowed to warm to room temperature. After 2.5 h, bromoacetonitrile (0.074 mL, 1.06 mmol) was added and the reaction mixture stirred at rt. After 17 h, NaH (60% dispersion in mineral oil, 0.085 mg, 2.12 mmol) and bromoacetonitrile (0.074 mL, 1.06 mmol) were added. After 2 h the reaction mixture was evaporated to dryness and the crude product purified on a Biotage Horizon HPFC system eluting with 5-90% EtOAc in petroleum ether (40-60° C.) to give the title compound (0.47 g, 42%) as an oil. 1H NMR (CDCl3): δ 4.46-4.40 (m, 1H), 4.24 (s, 2H), 4.17 (dd, 2H), 3.92 (dd, 2H), 1.45 (s, 9H); 13C NMR (CDCl3): δ 156.3, 115.6, 80.2, 69.3, 56.3, 54.6, 28.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960380B2
Source datasetuspto-grants-2011_06
ORD IDord-eb4ca9f37b9e4a87bfb3ec477a5332f1
Source noteuspto-grants-2011_06