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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973007Generated: October 29, 2026

Potassium Hydroxide → Tert-butyl 1-(2-fluorobenzyl)-2-isopropylidenehydrazinecarboxylate

https://huagongshe.com/reaction/1973007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactantalpha-Bromo-o-fluorotolueneHCID 67968—
ReactantN'-(propan-2-ylidene)(tert-butoxy)carbohydrazideHCID 11435207—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTolueneHCID 1140—
ProductTert-butyl 1-(2-fluorobenzyl)-2-isopropylidenehydrazinecarboxylateHCID 58529833105.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

Powdered KOH (4.24 g, 75.48 mmol) and tetrabutylammonium hydrogen sulfate (1.97 g, 5.81 mmol) were added to a solution of tert-butyl 2-isopropylidenehydrazinecarboxylate (10 g, 58.05 mmol) in toluene (150 mL). The mixture was stirred vigorously and heated to 50° C. and 1-(bromomethyl)-2-fluorobenzene (13.17 g, 69.68 mmol) was added slowly. The temperature was increased to 80° C. and maintained for 3 h and cooled to room temperature. The mixture was washed with water until the pH of the aqueous wash was neutral. The organic layer was washed with brine and dried over MgSO4 and concentrated to give a yellow oil (17.11 g) used for the next step without further purification). LC-MS [M+H]+=280.9, RT=3.41 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-e2f294fa6ace452888e25804b873d07c
Source noteuspto-grants-2013_04