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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193071Generated: October 26, 2026

Toluene → 3,6-Diaza-bicyclo(3.2.0)heptane-6-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1193071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl (2,2-dimethoxyethyl)carbamateHCID 10800009—
ReactantBenzyl allyl(2,2-dimethoxyethyl)carbamateHCID 11044136—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
Product3,6-Diaza-bicyclo(3.2.0)heptane-6-carboxylic acid tert-butyl esterHCID 4673818198%

Reaction Conditions

Temperature50 °C

Reaction Steps

Allyl-(2,2-dimethoxy-ethyl)-carbamic acid benzyl ester. To a 500 mL round-bottomed flask equipped with thermocouple probe, nitrogen inlet, reflux condenser, heating mantle, and mechanical stirring was added (2,2-dimethoxy-ethyl)-carbamic acid benzyl ester (50 g, 209 mmol) in toluene (180 mL). To the resulting solution was added powdered KOH (51.6 g, 920 mmol) and triethylbenzylammonium chloride (0.810 g, 3.55 mmol). A solution of allyl bromide (33.0 g, 275 mmol) in toluene (50 mL) was added dropwise over 10 minutes. The mixture was heated to 50° C. and stirred for 2 days. To the reaction mixture was added water (230 mL) over ten minutes. The layers were separated and the aqueous was extracted with toluene (2×200 mL). The combined organics were washed with brine (1×200 mL), dried with magnesium sulfate, filtered, and concentrated to afford the title compound (57.8 g, 98%). 1H-NMR (CDCl3, 500 MHz): 7.31 (m, 5H), 5.76 (m, 1H), 5.15 (m, 4H), 4.51 (m, 1H), 3.98 (d, J=9.48, 2H), 3.36 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680275B2
Source datasetuspto-grants-2014_03
ORD IDord-4c93df1c45a04348909210ea2e369b11
Source noteuspto-grants-2014_03