HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643874Generated: October 30, 2026
Sodium Carbonate → 5-(3-Benzyloxy-7-vinylnaphthalen-2-yl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one
https://huagongshe.com/reaction/643874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dibutyl Vinylboronate (stabilized with Phenothiazine) | HCID 236543 | — |
| Reactant | 5-(3-(Benzyloxy)-7-bromonaphthalen-2-yl)-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 66750633 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 5-(3-Benzyloxy-7-vinylnaphthalen-2-yl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one | HCID 66750637 | — |
Reaction Steps
To a microwave vial containing 5-(3-benzyloxy-7-bromonaphthalen-2-yl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (Example 3, step D) (0.21 g, 0.46 mmol), vinylboronic acid dibutyl ester (0.20 mL, 0.92 mmol), and PS-tetrakistriphenylphosphine palladium (0.36 mg, 0.046 mmol) in DME (4 mL) is added Na2CO3 (2.0M, 0.92 mL, 1.83 mmol). This is stirred in the microwave at 110° C. for 10 min, at which time LC/MS reveals complete conversion to the desired product. The resin-bound palladium is removed by filtration and the filtrate is concentrated in vacuo, and purified by reverse-phase Biotage MPLC to afford 5-(3-benzyloxy-7-vinylnaphthalen-2-yl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one as a light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700633B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-7f6b9c684e8b463f941fa3921bd17bb1 |
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| Source note | uspto-grants-2010_04 |
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