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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzyl (2,2-dimethoxyethyl)carbamate | HCID 10800009 | — |
| Reactant | Benzyl allyl(2,2-dimethoxyethyl)carbamate | HCID 11044136 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,6-Diaza-bicyclo(3.2.0)heptane-6-carboxylic acid tert-butyl ester | HCID 46738181 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680275B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-4c93df1c45a04348909210ea2e369b11 |
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| Source note | uspto-grants-2014_03 |
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