HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835513Generated: October 28, 2026
Benzenethiol, 2-amino-4-chloro-, hydrochloride (1:1) → HCID 22148788, compound
https://huagongshe.com/reaction/1835513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenethiol, 2-amino-4-chloro-, hydrochloride (1:1) | HCID 521980 | — |
| Reactant | HCID 22148797 | HCID 22148797 | — |
| Reactant | Phosphorus Pentoxide-Methanesulfonic Acid | HCID 86584057 | — |
| Product | HCID 22148788 | HCID 22148788 | 99% |
Reaction Steps
By a modification of the procedure of D. L. Boger (J. Org. Chem. 43, 2296-2297 (1978) a solution of P2O5/MeSO3H (Aldrich, 7.5 g, 1:10, w:w) was treated with 2-amino-4-chloro-benzenethiol hydrochloride (example 112, 1.96 g, 10.0 mmol) and (2,6-dichloro-4-nitro-phenyl)-acetic acid (example 110, 2.50 g, 10.0 mmol). The resulting mixture was stirred at room temperature for 1 hour, then heated at 90° C. overnight (15 hours). After cooled to room temperature, the reaction mixture was poured to ice and the resulting mixture was extracted 3× with EtOAc (50 mL). The organic layers were combined and washed twice with a brine solution (100 mL), dried over Na2SO4, and concentrated under vacuum. The crude solid was chromatographed (CH2Cl2) to yield 3.7 g (99%) of compound 114 as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770648B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-36c101079509447d90ebef373faceb4d |
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| Source note | uspto-grants-2004_08 |
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