HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594875Generated: October 28, 2026
Ethyl bromodifluoroacetate → HCID 86724272, compound
https://huagongshe.com/reaction/594875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | HCID 86724254 | HCID 86724254 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Ether tetrahydrofuran | HCID 21868444 | — |
| Product | HCID 86724272 | HCID 86724272 | 96.6% |
Reaction Steps
To a suspension of activated zinc (3.44 g, 52.5 mmol) in Et2O-THF (50% v/v, 80 ml) under reflux was slowly added a solution of ethyl bromodifluoroacetate (8.00 g, 39.4 mmol) and N-(6-bromo-4H-spiro[chromene-3,1′-cyclopropan]-4-ylidene)-2-methylpropane-2-sulfinamide (4.68 g, 13.1 mmol) in Et2O-THF (50% v/v, 80 ml) over 40 minutes, and the mixture was stirred for 4 hours at the same temperature. After cooling, the mixture was filtrated through celite pad and washed with EtOAc. To the filtrate were added saturated aqueous NH4Cl and EtOAc. After separation, the water layer was extracted with EtOAc. The combined organic layer was dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography (EtOAc:hexane=20:80-100:0) to give ethyl {6-bromo-4-[(tert-butylsulfinyl)amino]-4H-spiro[chromene-3,1′-cyclopropan]-4-yl}(difluoro)acetate (6.08 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242973B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-8413a7853cc442e2b456c38b8d1522b7 |
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| Source note | uspto-grants-2016_01 |
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