HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573000Generated: October 29, 2026
Sodium Hydroxide → HCID 58852716, compound
https://huagongshe.com/reaction/573000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 58852670 | HCID 58852670 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 58852716 | HCID 58852716 | 73.7% |
Reaction Steps
117.3 ml (888 mmol) of DAST were added dropwise over the course of 30 min. to a solution, cooled to 10° C., of 105.9 g (296 mmol) of 1,1-bis(6-bromo-2-pyridyl)ethan-1-ol in 1500 ml of chloroform at such a rate that the temperature did not exceed 20° C. The reaction mixture was stirred at 20° C. for 1 h and then hydrolysed dropwise with 500 ml of ice-water (care: highly exothermic reaction) with ice cooling and subsequently with 1000 ml of aqueous 3M NaOH. The organic phase was separated off, the aqueous phase was extracted twice with 100 ml of chloroform, and the combined organic phases were washed once with 500 ml of water and dried over calcium chloride. After the desiccant had been filtered off, the brown organic phase was concentrated to 200 ml and filtered through a silica-gel column. The yellow solution obtained in this way was evaporated to dryness, and the yellow, viscous oil remaining was recrystallised from 200 ml of n-heptane, giving 78.6 g (218 mmol) of the product, corresponding to a yield of 73.7%, in the form of colourless crystal needles—purity according to 1H-NMR>99.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029539B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-5c25743126c343169b067664c7bea5f3 |
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| Source note | uspto-grants-2015_05 |
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