HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226205Generated: October 30, 2026
tert-Butyldimethylsilyl chloride → HCID 54208717, compound
https://huagongshe.com/reaction/226205
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2-(2-Hydroxyethyl)-6-nitro-2H-1,4-benzoxazin-3(4H)-one | HCID 3740138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | N,N-Diethyl-2-propanamine | HCID 521913 | — |
| Product | HCID 54208717 | HCID 54208717 | 14.1% |
Reaction Steps
To solution of 4.8 g racemic-2-(2-hydroxyethyl)-6-nitro-3-oxo-4H-benz[1,4]oxazine in dimethylformamide (100 mL) and 3.4 mL diethylisopropylamine at 0° C. was added 4.7 g tert-butyldimethylsilylchloride. The reaction mixture was stirred at 0° C. for 20 minutes, at room temperature for 3 hour, concentrated and the resulting residue was partitioned between sodium bicarbonate solution and EtOAc. The aqueous phase was extracted with EtOAc and the combined organics washed with water, brine then dried over MgSO4. The solvent was removed by in vacuo and the crude material purified by column chromatography (hexanes/EtOAc) to yield 1 g of the desired product racemic-2-(2-t-butyldimethylsiloxyethyl)-6-nitro-3-oxo-4H-benz[1,4]oxazine MS (m/e): 353 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557207B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-fd3d709aecdc40f99a1ec7958cd30c28 |
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| Source note | uspto-grants-2009_07 |
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