HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622370Generated: October 30, 2026
Sodium hydride → (S)-methyl 3,4-dihydro-2,8-diisopropyl-3-oxo-2H-1,4-benzoxazine-4-acetate
https://huagongshe.com/reaction/622370
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | (S)-2,8-diisopropyl-2H-1,4-benzoxazin-3(4H)-one | HCID 7210282 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-methyl 3,4-dihydro-2,8-diisopropyl-3-oxo-2H-1,4-benzoxazine-4-acetate | HCID 14234720 | 81.1% |
Reaction Steps
To a solution of (S)-2,8-diisopropyl-2H-1,4-benzoxazin-3(4H)-one (4.66 g) in dimethylformamide (60 ml), was added portionwise 60% sodium hydride in oil (0.84 g). The mixture was stirred at room temperature for 10 minutes, and a solution of methyl bromoacetate (2.0 ml) in dimethylformamide (6.0 ml) was added thereto. The whole was stirred at room temperature for 30 minutes, diluted with water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and concentrated. The residue was crystallized from hexane to yield (S)-methyl 3,4-dihydro-2,8-diisopropyl-3-oxo-2H-1,4-benzoxazine-4-acetate as crystals (4.95 g, 81.1%). Recrystallization from hexane gave colorless needles, mp 67°-68° C. [α]D23 +3.7° (c=0.95, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04771050 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-9eabbaab1b31466eb8745f192c8983cf |
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| Source note | uspto-grants-1988_09 |
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