HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384079Generated: October 30, 2026
tert-Butanol → tert-Butyl ((3-(3-bromophenyl)oxetan-3-yl)methyl)carbamate
https://huagongshe.com/reaction/384079
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acid | HCID 57969737 | — |
| Product | tert-Butyl ((3-(3-bromophenyl)oxetan-3-yl)methyl)carbamate | HCID 57969817 | 45% |
Reaction Steps
2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acid (840 mg, 2.789 mmol) was dissolved in tert-butanol (8 mL) and triethylamine (310.5 mg, 427.7 μL, 3.068 mmol) was added followed by diphenylphosphoryl azide (844.3 mg, 661.2 μL, 3.068 mmol). Heat at 80° C. for 4 hours. The reaction was allowed to cool and the solvent removed under reduced pressure. Ethyl acetate was added and the organic layer was washed with 5% citric acid soln, NaHCO3 (sat. aq. soln.) and brine. The organics were dried over MgSO4, filtered and the solvent removed under reduced pressure. The crude product was pre-adsorbed onto silica and purified (Companion, 40 g) eluting with 2.5-50% EtOAc:Petrol ether to give tert-butyl N-[[3-(3-bromophenyl)oxetan-3-yl]methyl]carbamate as a white solid (433 mg, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367697B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-a73a310f79644aefbf02267e0ad1bf99 |
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| Source note | uspto-grants-2013_02 |
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