HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → HCID 25056514, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(Chloromethyl)benzoic acid | HCID 241752 | — |
| Reactant | HCID 25056515 | HCID 25056515 | — |
| Product | HCID 25056514 | HCID 25056514 | — |
Reaction Steps
The reaction of allyl alcohol and 3-chloromethyl-benzoic acid in the presence of sodium hydride was performed as described for Compound 37 to give 3-Allyloxymethyl-benzoic acid as colorless oil. 1H-NMR (400 MHz, d6-DMSO): 7.90 (m, 1 arom.H); 7.85 (m, 1 arom.H); 7.55 (m, 1 arom.H); 7.47 (m, 1 arom.H); 5.92 (m, —CH═CH2); 5.30, 5.16 (2 d-like, —CH═CH2); 4.52 (s, —OCH2—C6H4); 4.00 (d-like, CH2═CHCH2O). 13C-NMR (100 MHz, d6-DMSO): 167.24 (—C═O); 138.98; 135.04; 131.77; 130.80; 128.56; 128.34; 128.14; 116.60; 70.70; 70.55.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466199B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-9832afb283f8407db77cb815aa3d7fff |
| Source note | uspto-grants-2013_06 |