HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621504Generated: November 2, 2026
Sodium Hydroxide → HCID 21243176, compound
https://huagongshe.com/reaction/621504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14074107 | HCID 14074107 | — |
| Reactant | HCID 15576452 | HCID 15576452 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21243176 | HCID 21243176 | 91.6% |
Reaction Steps
A mixture of 3.605 g (10 mmol) of 1-(4-hydroxyphenyl)-4-(2-methyl-4-(4-tolyl)pyrimidin-6-yl)piperazine, 80 ml of toluene, 4.20 g (10 mmol) of 2-bromomethyl-2-(2,4 -dichlorophenyl)-4-methanesulfonyloxymethyl-1,3-dioxolane (cis/trans mixture), 0.65 g of tetrabutylammonium bromide and 13.5 ml of 50% strength sodium hydroxide solution was stirred vigorously for 4 hours at 55° C. The phases were subsequently separated at room temperature, the sodium hydroxide solution was extracted by shaking three times with ether, and the tolune and ther phases were combined. These were washed three times with water, dried, filtered and evaporated in vacuo. The residue remaining (7.4 g) was chromatographed on a silica gel S/CH2Cl2 column (diameter 2.6 cm, height 11 cm) with elution using CH2Cl2. After elution, the fractions which were unary according to TLC were combined and evaporated in vacuo. 6.27 g (=91.6% yield) of 2-bromomethyl-2 -(2,4-dichlorophenyl)-4-[4-(4-(2-methyl-4-(4-tolyl)pyrimidin-6-yl)piperazin-1-yl)phenoxymethyl]-1,3-dioxolane (cis/trans mixture) were obtained as a highly viscous oil;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824846 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-1dad5e0ea8a444f19f6c3be0c82d5721 |
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| Source note | uspto-grants-1989_04 |
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