HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 19746266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Bromomethylstyrene | HCID 98116 | — |
| Reactant | HCID 19746283 | HCID 19746283 | — |
| Reactant | HCID 19746287 | HCID 19746287 | — |
| Product | HCID 19746266 | HCID 19746266 | — |
| Product | HCID 19746277 | HCID 19746277 | — |
Reaction Steps
When the procedure of Example 1 is followed and benzyl bromide or phenethyl bromide are used in place of cinnamylbromide in Step G, then the products prepared are 1,3-di-(carbomethoxymethyl)-5-benzyloxybenzene and 1,3-di-(carbomethoxymethyl)-5-phenethyloxybenzene. These compounds are hydrolyzed in the same manner as Example 1, Step H to obtain 1,3-di-(carboxymethyl)-5-benzyloxybenzene and 1,3-di-(carboxymethyl)-5-phenethyloxybenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05232948 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-7b4d64dc68864eb5a2ea9556d7b2baae |
| Source note | uspto-grants-1993_08 |