HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486902Generated: October 27, 2026
Sodium Hydroxide → 2-(1,3-Benzodioxol-5-yl)ethanethiol
https://huagongshe.com/reaction/486902
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 3,4-Methylenedioxyphenethyl bromide | HCID 12207224 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1,3-Benzodioxol-5-yl)ethanethiol | HCID 15819512 | 95.5% |
Reaction Steps
750 g of 5-(2-bromoethyl)-1,3-benzodioxole was dissolved in 1 l of ethanol. 312 g of thiourea was added to the solution and the mixture was heated under reflux on a boiling water bath for 2 h. The reaction mixture was cooled. A solution of 300 g of sodium hydroxide in 1 l of water was added thereto and the mixture was heated under reflux on a boiling water bath for 45 min. After cooling, 3 l of water was added thereto and the product was extracted with 5 l of ethyl acetate. The extract was washed with dilute hydrochloric acid. It was then washed with water until the washing became substantially neutral and dried over anhydrous sodium sulfate. The solvent was distilled off at 40° C. to obtain about 570 g of a faint yellow oil. It was purified according to column chromatography with about 3 kg of silica gel (hexane:benzene=2:1) to obtain 310 g of the intended compound in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292901 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-b5d3b36d1eb444e981b16ace5af2720b |
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| Source note | uspto-grants-1994_03 |
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