HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372540Generated: October 30, 2026
Sodium Chloride → 7-dimethylamino-5-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene
https://huagongshe.com/reaction/372540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 7-dimethylamino-5-oxo-6,7,8,9-tetrahydro [5H] benzocycloheptene | HCID 54467523 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-dimethylamino-5-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene | HCID 20384438 | 91.1% |
Reaction Steps
A solution of 8.7 g of sodium borohydride in 87 ml of water was added to a solution of 8.7 g of the product of Step A in 435 ml of ethanol and the mixture was stirred at 20° C for 11/2 hours and was then poured into ice water. The mixture was saturated with sodium chloride and was extracted with ethyl acetate. The organic phase was washed with aqueous sodium chloride solution, was dried and evaporated to dryness to obtain 8 g of raw 7-dimethylamino-5-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene which was used as is for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04091115 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-0fa9f34a0f62490caf88cb36b997cfeb |
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| Source note | uspto-grants-1978_05 |
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