HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481516Generated: October 26, 2026
Methanol → 3-(4-Methoxyphenyl)-3-methylbutyronitrile
https://huagongshe.com/reaction/481516
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-(4-Methoxyphenyl)-2-methylpropanal | HCID 11137689 | — |
| Reactant | 1-Isocyanatomethanesulfonyl-4-methylbenzene | HCID 11789078 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3-(4-Methoxyphenyl)-3-methylbutyronitrile | HCID 19066479 | 60% |
Reaction Steps
To a mixture of KOBu-t (450 mg, 4.2 mmol) and TosCH2NCO (410 mg, 2.1 mmol) in DME (8 ml) was added a solution of Compound 45 (350 mg, 2.0 mmol) in DME (2 ml) with cooling (-40° C.). The mixture was stirred at same temperature for 10 min. and then at room temperature for 1 h and to this was added MeOH (6 ml) dropwise. The mixture was stirred at same temperature for 1 hr. and then at room temperature for 15 h. The mixture was concentrated to give a solid, which was dissolved in water (10 ml). The aqueous layer was extracted with CH2Cl2. The combined extracts were dried (Na2SO4) and concentrated in vacuo to give crude product (480 mg) as a yellow oil. The crude product was purified by a column chromatography to give Compound 46 (230 mg, 1.2 mmol,. 60%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05789423 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-eb4fc9b2b2924b63954a0817e631cf3f |
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| Source note | uspto-grants-1998_08 |
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