HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470656Generated: October 29, 2026
Acetyl chloride → 1-(3,3-Dimethyl-6-nitroindolin-1-yl)ethanone
https://huagongshe.com/reaction/470656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,3-Dimethyl-6-nitroindoline | HCID 21959466 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3,3-Dimethyl-6-nitroindolin-1-yl)ethanone | HCID 16127418 | — |
Reaction Steps
A solution of 3,3-dimethyl-6-nitroindoline (Example 4, 190.5 g) in 1200 mL IPAC, Et3N (200.6 g) was charged to a 1-L jacketed reactor, followed by the drop-wise addition of acetyl chloride (155.4 g) while maintaining reaction temperature<25° C. The reaction contents were stirred for 1 h at 20-25° C. 1200 mL D.I. water was charged slowly at T<30° C. to form a suspension. The product was isolated by filtration. Wet cake was washed with D.I. water (200 mL×2) and heptane (200 mL), and was dried at 50° C. under vacuum until constant weight. (193 g, 83.2 wt % adjusted yield, 99.15 A %, 99.5 wt % (dry))
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629289B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-c6dc6292a01f47269daaf8809e5c4229 |
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| Source note | uspto-grants-2014_01 |
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