HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200186Generated: November 1, 2026
Chloroform → 2-(1-Bromocyclohexyl)-8-cyanomethyl-4-oxo-4H-[1]-benzopyran
https://huagongshe.com/reaction/1200186
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-(1-Bromocyclohexyl)-8-bromomethyl-4-oxo-4H-[1]-benzopyran | HCID 14650439 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1-Bromocyclohexyl)-8-cyanomethyl-4-oxo-4H-[1]-benzopyran | HCID 14650444 | 72.2% |
Reaction Steps
NaCN (3.88 g, 0.075 mole) was dissolved in water (11 ml) and to the solution was added benzyltrimethylammonium chloride (13.9 g, 0.075 mole). After stirring at 50° C. for 15 minutes, chloroform (120 ml) was added and further 2 -(1-bromocyclohexyl)-8-bromomethyl-4-oxo-4H-[1]-benzopyran (12 g, 0.03 mole) was added. The mixture was stirred for 4 hours. The chloroform layer was washed with water, dried (MgSO4) and then concentrated under reduced pressure to obtain crystals. The crude crystals were recrystallized from ethyl acetate to obtain the title compound (7.5 g) as prisms, m.p. 143°-144° C., yield 72.2%. IR and NMR spectra of this compound were identical with those of the compound obtained in Reference Example 20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04904690 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-df6218633a364984a6efef2022b93e8d |
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| Source note | uspto-grants-1990_02 |
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