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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627245Generated: October 25, 2026

(S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-ylcarbamate → (S)-1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-amine

https://huagongshe.com/reaction/627245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-ylcarbamateHCID 89852294—
CatalystZinc bromideHCID 10421208—
SolventDichloromethaneHCID 6344—
Product(S)-1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-amineHCID 8985132496.3%

Reaction Steps

To a solution of (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-ylcarbamate (Intermediate 233, 6.77 g, 19.82 mmol) in DCM (100 mL) at room temperature was added zinc bromide (17.86 g, 79.28 mmol). The reaction mixture was stirred overnight at room temperature. Another 1 eq of zinc bromide was added. After several hours the reaction mixture was filtered and washed with saturated sodium bicarbonate. The resulting emulsion was filtered through a nylon filter and the layers were separated. The organics were dried over magnesium sulfate, filtered and concentrated to afford the title compound as a yellow oil (4.61 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309245B2
Source datasetuspto-grants-2016_04
ORD IDord-dfe8c30f604f4108b5903b45896d8c99
Source noteuspto-grants-2016_04