HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376229Generated: October 27, 2026
p-Toluenesulfonic acid → Ethyl 2-[5,7-di(t-butyl)benzothiazolyl]acetate
https://huagongshe.com/reaction/376229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,5-Bis(tert-butyl)benzoic acid | HCID 85339 | — |
| Reactant | 3,5-Di(t-butyl)-2-mercaptoaniline | HCID 12087014 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 2-[5,7-di(t-butyl)benzothiazolyl]acetate | HCID 19360973 | — |
Reaction Steps
A mixture of 40 g of 3,5-di(t-butyl)-2-mercaptoaniline [prepared according to a literature procedure from 3,5-di(t-butyl)benzoic acid] and 75 mL of ethyl 3-(trimethoxy)propionate in 1.2 L of methanol containing 1.5 g of p-toluenesulfonic acid was stirred at r.t. for 18 h. Excess methanol was removed by rotary evaporation. The precipitated the solid was filtered and washed with cold methanol. The crude product was purified by flash chromatography on silica gel and eluted with heptane to give 20 g of ethyl 2-[5,7-di(t-butyl)benzothiazolyl]acetate. The latter was refluxed with 16 g of 1,1,7,7-tetramethyl-8-hydroxy-9-formyljulolidine in 200 mL of acetonitrile containing 4 mL of piperidine for 18 h. The reaction mixture was cooled and the precipitated bright orange solid was filtered to give 13 g of the desired dye C-545TB: m.p. 275-276° C.; Tg=140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06020078 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-7b439c4485154a7787245cc35d75960c |
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| Source note | uspto-grants-2000_02 |
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