HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888511Generated: October 26, 2026
2,2,2-Trifluoroethanethiol → HCID 58372853, compound
https://huagongshe.com/reaction/888511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanethiol | HCID 4133924 | — |
| Reactant | HCID 58372805 | HCID 58372805 | — |
| Reactant | [3-(2-Formyl-4-nitro-phenoxy)-5-trifluoromethyl-phenyl]acetic acid ethyl ester | HCID 58372860 | — |
| Product | HCID 58372853 | HCID 58372853 | — |
Reaction Steps
[3-(2-Formyl-4-nitro-phenoxy)-5-trifluoromethyl-phenyl]acetic acid ethyl ester was reduced to [3-(2-hydroxymethyl-4-nitro-phenoxy)-5-trifluoromethyl-phenyl]-acetic acid ethyl ester according to the procedure described in Example 21, Step 6 and then brominated as described in Example 21, Step 7 and then treated with 2,2,2-trifluoroethanethiol to give {3-[4-Nitro-2-(2,2,2-trifluoro-ethylsulfanylmethyl)-phenoxy]-5-trifluoromethyl-phenyl}-acetic acid ethyl ester. The amine was reduced as described in Example 21, Step 9, and then treated with pivaloyl chloride as described in Example 21, Step 10 to provide {3-[4-(2,2-Dimethyl-propionylamino)-2-(2,2,2-trifluoro-ethylsulfanylmethyl)-phenoxy]-5-trifluoromethyl-phenyl}-acetic acid ethyl ester. Hydrolysis of the ester as described in Example 21, Step 11 provided the acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247602B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-55f178a91cca48bf8c576ed73a7b7fbe |
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| Source note | uspto-grants-2012_08 |
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