Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 4-Thioureidoanisole | HCID 667549 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Amino-6-methoxybenzothiazole | HCID 15630 | — |
Reaction Steps
182 parts of p-methoxyphenyl-thiourea are suspended in ethylene chloride, and dehydrated, as described in Example 1. 35.5 parts of chlorine gas are then passed in over 1 hour at 20° C., but without addition of bromine. After stirring for a further hour, 6 parts of bromine are added, the mixture is heated to 40° C., and a further 35.5 parts of chlorine gas are introduced at this temperature over one hour. The reaction product is isolated as described in Example 1. 168 parts of 6-methoxy-2-amino-benzothiazole of melting point 160°-163° C. are thus obtained, corresponding to 93% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04113732 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-a2d5469e99a244ad8b6a5085cde22ce0 |
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| Source note | uspto-grants-1978_09 |
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