HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 14350160, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methyl 5-hydroxyhept-6-ynoate | HCID 14444695 | — |
| Reactant | HCID 14677849 | HCID 14677849 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 14350160 | HCID 14350160 | 129.2% |
Reaction Steps
Into a heavy walled pyrex test tube was added 130 mg (0.43 mmol) of 1-(0-bromophenyl)-1-nonanol, 67 mg (0.43 mmol) of methyl 5-hydroxy-6-heptynoate prepared according to the procedure of Nicolaou et al., J.A.C.S., 106, 2748 (1984), 25 mg (0.02 mmol, 5 mole%) of Pd(PPh3)4, and 4 ml (93.0 mg) of diisopropylamine. The reaction was run and worked up according to the procedure of Example 11 to yield 208 mg of a yellow-brown oil. The oil was chromatographed on a silica gel column which was eluted with 70% diethyl ether/hexane to produce the titled product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791133 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-c379ae8141b64759aafad911931137eb |
| Source note | uspto-grants-1988_12 |