HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357255Generated: October 31, 2026
Methanesulfonyl chloride → HCID 88429211, compound
https://huagongshe.com/reaction/357255
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4,10-Dihydro-10-oxothieno(3,2-c)(1)-benzoxepin-8-yl)butanol | HCID 135166 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 88429211 | HCID 88429211 | 10.8% |
Reaction Steps
A chilled stirring solution of 9.5 g of 4-(4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-yl)butanol in 200 ml of sieve dried pyridine was treated dropwise with 3.80 g of methanesulfonyl chloride and the addition funnel was rinsed with a few ml of methylene chloride. The stirring solution was allowed to equilibrate to room temperature overnight with the bath in place. The resulting solution was poured into 750 ml of water and was allowed to stand for 15 min. The solids were collected by filtration, and dried in vacuo overnight at 42°0 C. Concentration of the mother liquor produced additional solids which were combined with the first crop and dried to give a total of 9.09 g of crude material. A 2.0 g portion of the product was recrystallized from hexane/ethyl acetate to give 1.3 g of 4-(4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-yl)butanol methanesulfonate, m.p. 97°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840749 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-75d99f42bfe04605af956ed2bdd660b5 |
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| Source note | uspto-grants-1998_11 |
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