HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342194Generated: October 29, 2026
Benzyl mercaptan → HCID 53916822, compound
https://huagongshe.com/reaction/342194
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanone, (4-bromophenyl)(2-fluoro-4-methoxyphenyl)- | HCID 11833815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53916822 | HCID 53916822 | — |
Reaction Steps
4.3 g of potassium tert. butylate are dissolved in 160 ml of THF and treated slowly with 4.5 ml of benzyl mercaptan. The suspension is stirred at RT and then treated with 10 g of (4-bromophenyl)-(2-fluoro-4-methoxy-phenyl)-methanone in 200 ml of THF. The solution is stirred at RT and treated with 100 ml of ammonium chloride solution as well as 200 ml of sodium hydrogen carbonate solution. The phases are separated, the inorganic phase is extracted with ethyl acetate and the organic phases are washed with sat. sodium hydrogen carbonate solution and sodium chloride solution and dried. There are obtained 15.8 g of (2-benzylsulphanyl-4-methoxyphenyl)-(4-bromo-phenyl)-methanone which are taken up in 160 ml of methylene chloride, treated with 3.4 ml of sulphuryl chloride and stirred at RT. After distillation of the sulphuryl chloride the residue is taken up in 160 ml of THF, treated with 120 ml of a saturated ammonia solution in ethanol and stirred. 100 ml of sodium hydrogen carbonate solution are added. The solvent is removed and the residue is again taken up in sodium hydrogen carbonate solution and ethyl acetate. The phases are separated and the inorganic phase is extracted with ethyl acetate and ether. The organic phases are washed with sodium chloride solution and dried. Recrystallization from ethyl acetate/ethanol yields 7.52 g of 3-(4-bromo-phenyl)-6-methoxy-[d]-benzisothiazole, MS: m/e 318 (M, 1 Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856503 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-c575e605028d4149aa713ba754586f21 |
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| Source note | uspto-grants-1999_01 |
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