HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485100Generated: October 31, 2026
Hydrochloric Acid → Dibenzo[b,f]thiepin-3-carboxaldehyde
https://huagongshe.com/reaction/485100
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 13490383 | HCID 13490383 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Dibenzo[b,f]thiepin-3-carboxaldehyde | HCID 13520244 | — |
Reaction Steps
Saturate a suspension of anhydrous stannous chloride (378 mg; 2 mmole) in 7.5 ml dry ether with hydrogen chloride at a temperature of 0°-5° C., and add 235 mg (1 mmole) of 3-cyano-dibenzo[b,f]thiepin. Stir for one hour at 0° C. and allow to warm to room temperature (25° C.). Continue stirring at room temperature for approximately 48 hours. Add 5 ml of water and 1 ml 2N hydrochloric acid, and extract with a mixture of 5 ml ether and 5 ml ethyl acetate. When the hydrolysis of the chloro stannate is complete, evidenced by the disappearance of solids from the solution, separate the organic layer containing the product, wash with water/sodium chloride solution, and after drying, evaporate the solution to produce a dark oil which solidifies when triturated with hexane. The title product is obtained when the above solid material is crystallized from acetonitrile, m.p. 114.5°-115.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04535171 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-43639821fbc44e9a973a8cd7a31486be |
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| Source note | uspto-grants-1985_08 |
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