HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromooctane → HCID 19375100, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19375135 | HCID 19375135 | — |
| Product | HCID 19375100 | HCID 19375100 | 87% |
Reaction Steps
This phenol is alkylated again by the same method, but using sodium hydride and 1-bromooctane, to provide 1-((2,2-dimethoxyethyl)thio)-4-(octyloxy)benzene as a colorless oil after chromatography (87% yield). By the method of example 2, this is converted into the title compound, obtained as a pale yellow solid, mp 70°-72° after recrystallization from hexane-dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464865 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-de59ee9f9e3c4d6db9719975f4bd7c6d |
| Source note | uspto-grants-1995_11 |