HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104129Generated: October 30, 2026
Sodium Azide → tert-Butyl [1-(4-bromophenyl)cyclobutyl]carbamate
https://huagongshe.com/reaction/2104129
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(4-Bromophenyl)cyclobutane-1-carboxylic acid | HCID 16769919 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | Zinc trifluoromethanesulfonate | HCID 104671 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl [1-(4-bromophenyl)cyclobutyl]carbamate | HCID 52988051 | — |
Reaction Steps
1-(4-bromophenyl)cyclobutanecarboxylic acid (7-1, 10.89 g, 42.7 mmol), Boc anhydride (10.90 mL, 47.0 mmol), sodium azide (9.71 g, 149 mmol), tetrabutylammonium bromide (2.048 mL, 6.40 mmol) and zinc trifluoromethansulfonate (0.155 g, 0.427 mmol) were stirred in THF (100 ml) at 60° for 4 h. The reaction mixture was cooled to room temperature and EtOAc and saturated aqueous sodium bicarbonate were added to the mixture. The suspension was filtered through a glass frit and the filtrate was extracted with EtOAc, washing with water and brine. The organic layer was dried over Na2SO4, filtered and reduced in vacuo to a tan oil. The crude product was purified by normal phase flash chromatography eluting with 5-15% EtOAc/Hex to give 7-2 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576209B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-b8c2819607184ac69034d983164d0dee |
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| Source note | uspto-grants-2009_08 |
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