HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Xylyl bromide → HCID 19801104, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | HCID 19801008 | HCID 19801008 | — |
| Product | HCID 19801104 | HCID 19801104 | 63.5% |
Reaction Steps
As in Example 54, 2-(1,2-epoxy-1,5-dimethyl-4-hexenyl)-3-methoxy-1-methylthiomethyl-1,4-cyclohexanediol (200 mg) was allowed to react with 4-methylbenzyl bromide (1.12 g) to give 2-(1,2-epoxy-1,5-dimethyl-4-hexenyl)-3-methoxy-1-(4-methylbenzyl)methylsulfoniomethyl-1,4-cyclohexanediol bromide (198 mg: yield 56%) as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05180735 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-de0579ba43754b0486fff9c9510ed784 |
| Source note | uspto-grants-1993_01 |