HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834544Generated: October 30, 2026
Hydrochloric Acid → Diisobutyl-n-heptyl-phosphine oxide
https://huagongshe.com/reaction/1834544
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylphosphinyl chloride | HCID 22481195 | — |
| Reactant | HCID 178443916 | HCID 178443916 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diisobutyl-n-heptyl-phosphine oxide | HCID 22481194 | — |
Reaction Steps
A solution of di-isobutylphosphinyl chloride* (3.9g., 0.02 mole) in tetrahydrofuran (50 ml.) was added dropwise to a refluxing solution of n-heptylmagnesium bromide (prepared from magnesium turnings (1.2g., 0.05 mole), n-heptyl bromide (9.0g., 0.05 mole) and tetrahydrofuran (100 ml.)). The mixture was heated under reflux for 18 hours. After cooling to room temperature, the reaction mixture was poured onto ice and 2N HCl (300 ml.), and extracted with methylene dichloride (4 × 200 ml.). The combined extracts were washed with lithium hypochlorite solution, 2N NaOH solution and finally with water, then dried (MgSO4). The solvent was removed by distillation and the residual yellow oil (8g.) was eluted with chloroform down a silica gel column. The product (Rf = 0.1- 0.2 on silica t.l.c. (CHCl3)) was finally distilled to yield diisobutyl-n-heptyl-phosphine oxide as a colourless liquid, bp. 120°-2°/0.03 mm. (Found C 68.8; H 13.0; C15H33OP requires C 69.3; H, 12.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04070496 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-e6cf7232ea8649b1a38435e3869382f2 |
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| Source note | uspto-grants-1978_01 |
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