HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-acetoxynonane → HCID 22615362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-acetoxynonane | HCID 13104716 | — |
| Reactant | HCID 54471702 | HCID 54471702 | — |
| Product | HCID 22615362 | HCID 22615362 | — |
Reaction Steps
The title compound was prepared from [3-(methanesulfonylamino-methyl)-phenoxy]-acetic acid methyl ester (Preparation 10) and acetic acid 1-(3-chloropropyl)-hexyl ester using the alkylabon procedure described in U.S. Pat. No. 4,033,996. 1H NMR (CDCl3) δ 7.31-7.26 (m, 1H), 7.02-6.84 (m, 3H), 4.68 (s, 2H), 4.35 (s, 2H), 3.91-3.89 (m, 1H), 3.20-3.12 (m, 2H), 2.83 (s, 3H), 1.94-1.92 (m,1H), 1.79-1.24 (m, 12H), 0.87 (t, 3H); MS 400 (M+−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376502B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-02ef360bd74e4f28b805b5465e5432b6 |
| Source note | uspto-grants-2002_04 |