HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103129Generated: October 26, 2026
4-Morpholinecarbonyl chloride → (6-Fluoro-2,2-diphenyl-benzo[1,3]dioxol-5-yl)-morpholin-4-yl-methanone
https://huagongshe.com/reaction/2103129
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Morpholinecarbonyl chloride | HCID 84810 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Bromo-6-fluoro-2,2-diphenyl-2H-1,3-benzodioxole | HCID 21865386 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (6-Fluoro-2,2-diphenyl-benzo[1,3]dioxol-5-yl)-morpholin-4-yl-methanone | HCID 10024236 | 68% |
Reaction Steps
To a cooled (−78° C.) solution of 5-bromo-6-fluoro-2,2-diphenyl-benzo[1,3]dioxole (17.59 g, 47.4 mmol) in diethyl ether (300 mL) was slowly added a solution of n-butyl lithium in hexanes (1.6M, 30 mL, 48 mmol, 1.0 eq.). The reaction mixture was stirred 1 h at −78° C. before the addition of 4-morpholinecarbonylchloride (8.5 g, 56.9 mmol, 1.2 eq.). The reaction mixture was allowed to warm to 20° C. and poured into an aqueous solution of sodium bicarbonate. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine. Volatiles were removed in vacuo. Purification by flash chromatography afforded the title compound (13.0 g, 68%) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576088B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-e97f4880170c49a0b9578021f8062a33 |
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| Source note | uspto-grants-2009_08 |
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