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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366739Generated: October 27, 2026

Imidazole → (R)-N-Boc-2-amino-1-(-tert-butyldimethylsilyloxy)-but-3-yne

https://huagongshe.com/reaction/366739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(R)-tert-Butyl (1-hydroxybut-3-yn-2-yl)carbamateHCID 10921216—
SolventDichloromethaneHCID 6344—
Product(R)-N-Boc-2-amino-1-(-tert-butyldimethylsilyloxy)-but-3-yneHCID 21971750—

Reaction Steps

To a solution of (R)-N-Boc-2-amino-but-3-yn-1-ol (150 mg, 0.81 mmol) (Example 104B) and imidazole (110 mg, 1.62 mmol) (Aldrich) in CH2Cl2 (10 mL) was added at 0° C. tert-butyldimethylsilyl chloride (146 mg, 0.97 mmol) (Fluka). After 5 min the reaction mixture was poured into H2O and extracted with CH2Cl2. The CH2Cl2 layer was dried over Na2SO4 and concentrated to a residue which after silica gel column chromatography with a 0-30% Et2O in hexanes gradient afforded the product. (Yield 210 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130239
Source datasetuspto-grants-2000_10
ORD IDord-7b386a728fce4a37a4fb901368071c38
Source noteuspto-grants-2000_10