HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 67071595, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 67071422 | HCID 67071422 | — |
| Product | HCID 67071595 | HCID 67071595 | — |
Reaction Steps
(E)-3-[1′-Methyl-4-oxo-spiro(chromane-2,3′-azetidine)-6-yl]-acrylic acid methyl ester was synthesized starting from Intermediate 4 (500 mg, 1.62 mmol), according to the procedure for preparation of Example 31, Step A, using aqueous 37% formaldehyde solution (0.088 ml, 3.2 mmol), and NaBH(OAc)3 (515 mg, 2.43 mmol). The product was obtained as pale yellow oil (430 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08980877B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-2e936b41091f4b47a506c3ceff515808 |
| Source note | uspto-grants-2015_03 |