HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199923Generated: October 31, 2026
Dimethyl Disulfide → HCID 19864321, compound
https://huagongshe.com/reaction/1199923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | HCID 19864294 | HCID 19864294 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19864321 | HCID 19864321 | — |
Reaction Steps
A solution of n-butyl lithium in n-hexane (1.6M, 0.75 ml) was added dropwise to a stirred solution of 2-bromo-6-methyl-8-phenyl-5,6,7,8-tetrahydro-4H-thieno[2,3-d]azepine (0.40 g hydrobromide salt converted to free base by aqueous ammonia/dichloromethane extraction) in dry tetrahydrofuran (10 ml) cooled to -70° under nitrogen. After 10 minutes at -70° dimethyl disulphide (0.11 ml) was added dropwise and the mixture allowed to warm to room temperature. After 30 minutes the solution was evaporated, water (10 ml) added to the residue and extracted with dichloromethane (2×5 ml). The extracts were dried, filtered and evaporated to a pale yellow solid. Recrystallisation twice from n-hexane (4 ml) gave white needles (m.p. 90°) of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04904653 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-9330217efbde41d89185d3505136336f |
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| Source note | uspto-grants-1990_02 |
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