HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401677Generated: October 31, 2026
Tetrahydro-4H-pyran-4-one → HCID 43608624, compound
https://huagongshe.com/reaction/2401677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydro-4H-pyran-4-one | HCID 121599 | — |
| Reactant | 4-Bromo-2-chloroaniline | HCID 610169 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 43608624 | HCID 43608624 | 86% |
Reaction Steps
A mixture of 4-bromo-2-chloro-phenylamine (4 g, 19.37 mmol), tetrahydro-4H-pyran-4-one (2.69 ml, 29.05 mmol), oven dried molecular sieves 4 Å (2 g) and sodium triacetoxyborohydride (6.12 g, 29.05 mmol) in 1,2-dichloroethane (100 ml) was stirred at room temperature for 72 hours. The mixture was filtered through a diatomaceous earth pad. The diatomaceous earth pad was washed with dichloromethane. The combined filtrates were washed with NaHCO3 (aqueous saturated solution), dried over Na2SO4 and evaporated till dryness. The crude product thus obtained was purified by column chromatography (silica gel; DCM to DCM/MeOH(NH3) up to 5%). The desired fractions were collected and evaporated in vacuo to yield intermediate 12 as a brown oil (4.83 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796311B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-28d67af522f44e1bbb55e57b4860c441 |
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| Source note | uspto-grants-2014_08 |
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