HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435425Generated: October 25, 2026
Diisopropylamine → 4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile
https://huagongshe.com/reaction/435425
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | 3-Methyl-2-butenenitrile | HCID 94301 | — |
| Reactant | 1-(Isopropylsulfonyl)-4-methylbenzene | HCID 816792 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile | HCID 12833028 | — |
Reaction Steps
3.81 ml of a cyclohexane solution of 1.75M of butyllithium were added at -30° to -40° C. to a mixture of 1.05 ml of diisopropylamine and 4 ml of tetrahydrofuran and the mixture was stirred for 10 minutes and was then cooled to -60° to -70° C. Then 1.22 g of p-tolyl isopropylsulfone were added to the mixture which after 15 minutes of contact was poured over 10 minutes under an inert atmosphere into a solution of 0.5 g of dimethylacrylonitrile and 4 ml of tetrahydrofuran at -60° to -70° C. The mixture was stirred for 30 minutes at -60° to -70° C. and was then poured into an aqueous saturated monosodium phosphate solution. The mixture was extracted with benzene and the organic phase was dried and evaporated to dryness. The residue was crystallized from isopropyl ether to obtain 0.740 g of 4-p-tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile melting at 126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04401601 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-65212fa3874a4fbfb05ef8243326a26e |
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| Source note | uspto-grants-1983_08 |
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