HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324504Generated: October 29, 2026
Sodium hydrosulfide → HCID 88151774, compound
https://huagongshe.com/reaction/324504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178503574 | HCID 178503574 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 88151774 | HCID 88151774 | — |
Reaction Steps
A solution of the product of example 39 step (i) (0.120 g) together with 2-bromoethyl methyl ether (0.073 ml) and a 1M solution of potassium tert-butoxide in tetrahydrofuran (0.62 ml) in N,N-dimethylformamide (3 ml) was heated at 50° C. for 20 h. Sufficient sodium hydrosulphide was added to give a blue solution and the reaction mixture heated at 80° C. for 4 h. The reaction mixture was cooled, diluted with ethyl acetate and washed with saturated aqueous ammonium chloride. The organic phase was dried over magnesium sulphate, filtered and evaporated. The crude product was purified by chromatography eluting with 1% methanol in dichloromethane, followed by trituration with ethyl acetate to give the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218376B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-7bd2ca4f6b7a4e06a8ac7f7d38531727 |
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| Source note | uspto-grants-2001_04 |
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