HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597786Generated: October 30, 2026
Ammonium Chloride → 1-(1,3-Benzothiazol-2-yl)ethan-1-ol
https://huagongshe.com/reaction/1597786
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,3-Benzothiazole-2-carbaldehyde | HCID 241608 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | 1-(1,3-Benzothiazol-2-yl)ethan-1-ol | HCID 2830674 | 66% |
Reaction Steps
5.0 ml of methylmagnesium bromide were added dropwise to a solution of 0.61 g of 2-formylbenzothiazole [prepared as described in step (a) above] which was cooled in an acetone-dry ice bath. The reaction vessel was transferred to an ice-water bath and the reaction mixture was stirred for 3.5 hours. At the end of this time, a saturated aqueous ammonium chloride solution was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The resulting extract was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the resulting residue was purified by column chromatography through silica gel using a 4:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.44 g (yield 66%) of the title compound as a solid having a melting point of 59° to 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05736487 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-f4359b0c2eed4677a40be68d6992f6bb |
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| Source note | uspto-grants-1998_04 |
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