HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347295Generated: October 29, 2026
4-Methoxy-alpha-toluenethiol → HCID 21924853, compound
https://huagongshe.com/reaction/347295
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxy-alpha-toluenethiol | HCID 80407 | — |
| Reactant | 12-Bromo-1-dodecanol | HCID 137895 | — |
| Reactant | Methoxide | HCID 3826051 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21924853 | HCID 21924853 | 90% |
Reaction Steps
Na (800 mg, 34.8 mmol) was dissolved in 30 mL of dry MeOH. Under argon, p-methoxybenzylmercaptan (2.75 mL, 3.04 g, 19.7 mmol) was added to the methoxide solution. After a few minutes, 12-bromododecanol (2.5 g, 9.43 mmol) was dropped into the reaction mixture. Within 5 minutes a solid began to come out of solution. After a minimum of 3 h, the reaction was filtered and washed 3× with cold MeOH, yielding 2.874 g (8.49 mmol, 90%) of pure product after drying. 1H NMR (CDCl3): d 7.23 (d, J=8.8 Hz, 2H, AA′ of AA′ BB′ aromatic system), 6.85 (d, J=8.8 Hz, 2H, BB′ of AA′ BB′ aromatic system), 3.80 (s, 3H, methoxy), 3.66 (s, 2H, benzyl), 3.64 (dt, J1=6.6 Hz, J2=5.5 Hz, 2H, RCH2OH), 2.40 (t, J=7.3 Hz, 2H, RSCH2R), 1.50–1.65 (cm, 4H, CH2 b to heteroatoms), 1.2–1.4 (cm, 16H, bulk methylenes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173130B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-96b3cf9eec9341c2a75d9f25788a4a8a |
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| Source note | uspto-grants-2007_02 |
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