HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633201Generated: October 27, 2026
(+)-Styrene oxide → (R)-methyl 2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoate
https://huagongshe.com/reaction/633201
Participants
| Role | Name | HCID | Charge |
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| Reactant | (+)-Styrene oxide | HCID 114705 | — |
| Reactant | Methyl 2-chloro-4-mercaptobenzoate | HCID 66877363 | — |
| Product | (R)-methyl 2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoate | HCID 66878702 | — |
Reaction Steps
150 mg of (R)-styrene oxide was reacted with methyl 2-chloro-4-mercaptobenzoate via Procedure S to afford (R)-methyl 2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoate. 190 mg of (R)-methyl-2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoate was hydrolyzed via Procedure M to give (R)-2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoic acid. 170 mg of (R)-2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoic acid was reacted via Procedure R to give (R)-2-chloro-4-(2-hydroxy-2-phenylethylsulfonyl)benzoic acid. 60 mg of 4-chloro-3-(pyridine-2-yl)aniline was coupled to (R)-2-chloro-4-(2-hydroxy-2-phenylethylsulfonyl)benzoic acid via Procedure G. The product was purified on reverse phase HPLC to yield (R)-2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(2-hydroxy-2-phenylethylsulfonyl)benzamide. MS (Q1) 527.2 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321761B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-9e3d98ef0ff04361bcbe9b21eea8a6f2 |
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| Source note | uspto-grants-2016_04 |
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