HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638940Generated: October 31, 2026
Potassium Hydroxide → 3,5-bis-dimethylthiocarbamoyloxybenzoic acid methyl ester
https://huagongshe.com/reaction/638940
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylthiocarbamoyl chloride | HCID 27871 | — |
| Reactant | Methyl 3,5-Dihydroxybenzoate | HCID 75076 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,5-bis-dimethylthiocarbamoyloxybenzoic acid methyl ester | HCID 12138348 | 63.8% |
Reaction Steps
To a stirred solution of 3,5-dihydroxybenzoic acid methyl ester (10.0 g, 59.5 mmol) in DMF (200 mL) at 0° C. was added NaH (60% dispersion in mineral oil, 5.00 g, 125 mmol, 2.1 eq.) in small portions. The reaction mixture was stirred at 0° C. for 15 min then warmed to room temperature. After 1 h, the reaction mixture was cooled to 0° C. and then added dimethylthiocarbamoyl chloride (14.7 g, 119 mmol). Following the addition, the reaction was stirred for 45 min at 0° C., then for 30 min at room temperature and then heated to 80° C. After 2 h at 80° C., the reaction mixture was cooled to room temperature and then added to 1% aqueous KOH (500 mL). The resulting mixture was extracted with ethyl ether (2×500 mL). The organic layer was washed with H2O (500 mL), brine (300 mL), dried over MgSO4 and concentrated in vacuo to afford 3,5-bis-dimethylthiocarbamoyloxybenzoic acid methyl ester (13.0 g). This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691843B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-f61fe97ace3247e383b854a5e2a40399 |
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| Source note | uspto-grants-2010_04 |
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