HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471916Generated: October 25, 2026
Sulfuric Acid → 2-Bromo-4-tert-butyl-5-nitrophenyl methyl carbonate
https://huagongshe.com/reaction/471916
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 2-Bromo-4-tert-butylphenyl methyl carbonate | HCID 59394944 | — |
| Product | 2-Bromo-4-tert-butyl-5-nitrophenyl methyl carbonate | HCID 59395050 | 76.1% |
Reaction Steps
2-Bromo-4-tert-butylphenyl methyl carbonate (5.0 g, 17.4 mmol) was added portion-wise to H2SO4 (9.3 mL, 174.1 mmol) to generate a colorless homogeneous solution. This solution was then cooled to 0° C. and treated with KNO3 (2.1 g, 20.9 mmol) portion-wise maintaining the internal temperature below 5° C. The reaction was stirred for 2 h and then poured on ice water. The aqueous layer was extracted with dichloromethane (3×10 mL). The combined organic extracts was dried over Na2SO4, filtered and concentrated. Purification by silica gel chromatography (10% ethyl acetate/hexane) provided 2-bromo-4-tert-butyl-5-nitrophenyl methyl carbonate (4.4 g, 76% yield). 1H NMR (400.0 MHz, DMSO-d6) δ 7.97 (s, 1H), 7.92 (s, 1H), 3.90 (s, 3H), 1.34 (d, J=5.4 Hz, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633189B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-3e2fdf4e1ad541c8a7d2d13fc80e101e |
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| Source note | uspto-grants-2014_01 |
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