Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 14674477 | HCID 14674477 | — |
| Product | HCID 20061587 | HCID 20061587 | — |
Reaction Steps
3-(2-tert-Butylthioethyl)-2-imino-6-trifluoromethoxybenzothiazoline hydrochloride (1.5 g) and 47% strength hydrobromic acid (15 cc) are heated for 4 hours to 100° C. After cooling of the mixture to 0° C., the precipitate formed is filtered off and washed with distilled water (2×25 cc) and then with ethyl ether (2×30 cc). 2-(2-Imino-6-trifluoromethoxy-3-benzothiazolinyl)ethanethiol hydrobromide (0.9 g), m.p. 180° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008280 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-271f7c3129ce4e0dbaa8a948ba53ea44 |
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| Source note | uspto-grants-1991_04 |
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