HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418806Generated: November 4, 2026
Boron trifluoride etherate → HCID 86753937, compound
https://huagongshe.com/reaction/1418806
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | HCID 54393632 | HCID 54393632 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86753937 | HCID 86753937 | — |
Reaction Steps
To a mixture of 0.60 g of 3,4-dihydro-5,8-dimethyl4-oxo-2H-1-benzothiopyran-6-carboxylic acid 1,1-dioxide in 30 mL of methylene chloride was added 0.24 mL of 1,2-ethanedithiol (purchased from Aldrich Chemical Co.) and 0.35 mL of boron trifluoride diethyl etherate (purchased from Janssen Chimica). The mixture was refluxed overnight and then concentrated under reduced pressure to dryness. To the resulting residue was added 10 mL of dilute hydrochloric acid of pH 1. The mixture was extracted with ethyl acetate, and the combined organic extracts were dried over MgSO4, filtered, and concentrated under reduced pressure to afford 0.62 g of the title compound of Step A as an orange solid which had a melting point >250° C. 1H NMR ((CD3)2SO): δ 2.65 (s, 3H), 2.77 (s, 3H), 2.94 (m, 2H), 3.55-3.80 (m, 6H), 7.50 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05885936 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-4c8d4adbc92548c7831c9eed2a4ecb85 |
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| Source note | uspto-grants-1999_03 |
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