HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405178Generated: October 30, 2026
Sodium methanethiolate → HCID 70976591, compound
https://huagongshe.com/reaction/1405178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 1-(Chloromethyl)-3-fluoro-5-nitrobenzene | HCID 56924386 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 70976591 | HCID 70976591 | 106.9% |
Reaction Steps
Sodium methanethiolate (1.22 g; 17.4 mmol) was added in three portions to a stirred solution of 1-(chloromethyl)-3-fluoro-5-nitrobenzene (3.00 g; 15.8 mmol, HE Chemical) in ethanol (33 ml) at 0° C. The ice bath was removed and the batch was stirred at room temperature for 18 hours. Further sodium methanethiolate (0.33 g; 4.7 mmol) was added and the batch was stirred for 5 additional hours at room temperature. The batch was diluted with brine and extracted with ethyl acetate (2×). The combined organic phases were washed with water, dried (sodium sulfate), filtered and concentrated to give the desired product (3.4 g) that was used without further purification. 1H NMR (400 MHz, CDCl3, 300K) δ=8.00 (m, 1H), 7.81 (m, 1H), 7.42 (m, 1H), 3.74 (s, 2H), 2.02 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916557B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-044237ca63384469b8f8bc7e3add210e |
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| Source note | uspto-grants-2014_12 |
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