HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966864Generated: October 30, 2026
Methanol → [5-(Butylsulfanyl)thiophen-2-yl]methanol
https://huagongshe.com/reaction/966864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86588308 | HCID 86588308 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | [5-(Butylsulfanyl)thiophen-2-yl]methanol | HCID 22292447 | — |
Reaction Steps
A solution of NaBH4 (5.3 g, 0.141 mol) in methanol (29.0 g) and sodium hydroxide (20%, 56.0 mL) was added dropwise to a solution of 45 (56.47 g, 0.282 mol) in THF (75 mL) at room temperature. The mixture was stirred for 2 hours, extracted with ethyl ether 3×150 mL), the combined extracts washed with brine and dried (MgSO4). After solvent removal, the crude product 46 was obtained as an oil (55.4 g, 97%); 1H NMR δ: 0.88 (t, 3 H, J=7.3 Hz, CH3), 1.39 (m, 2 H, CH3—CH2), 1.57 (m, 2 H, CH3—CH2—CH2),1.88 (s, 1 H OH), 2.76 (t, 2 H, J=7.3 Hz, CH2—S), 4.73 (s, 2 H, CH2—OH), 6.83 (d, 1 H, J=3.5 Hz, aromatic H), 6.94 (d, 1 H, J=3.5 Hz, aromatic H); λmax/nm (εmax/dm3 mol−1cm−1) 275.5 (3600); LRMS(EI+) calc. for C9H14OS2: 202.1, found 202.1. The product was used without further purification in the preparation of 47.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953570B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-39088f566e7c48dc9ce43205bf4571ef |
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| Source note | uspto-grants-2005_10 |
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