HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840448Generated: October 31, 2026
Ammonium Chloride → alpha-Trimethylsilylethynyl-4,4-dimethyl-6-thiochromanmethanol
https://huagongshe.com/reaction/840448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 4,4-dimethyl-3,4-dihydro-2H-thiochromene-6-carbaldehyde | HCID 15284308 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | alpha-Trimethylsilylethynyl-4,4-dimethyl-6-thiochromanmethanol | HCID 22361487 | 100% |
Reaction Steps
3 ml (21.3 mmol) of trimethylsilylacetylene and 50 ml of THF were introduced into a three-necked flask. A solution of 8.6 ml (21.3 mmol) of n-butyllithium (2.5M in hexane) was added dropwise at −78° C. under a stream of nitrogen and the reaction mixture was permitted to heat to room temperature. This solution was introduced dropwise into a solution of 4 g (19.4 mmol) of 4,4-dimethyl-6-thiochromancarboxaldehyde in 50 ml of THF at −78° C. The reaction mixture was permitted to heat to room temperature, was poured into an aqueous ammonium chloride solution and extracted with ethyl ether. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. 5.9 g (100%) of the expected alcohol were obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06368608B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-22ca85786dc54007b7021d2f324c09eb |
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| Source note | uspto-grants-2002_04 |
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