HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268139Generated: November 1, 2026
gamma-Hexalactone → HEXANAMIDE, 4-HYDROXY-N-[(4-METHOXYPHENYL)METHYL]-
https://huagongshe.com/reaction/2268139
Participants
| Role | Name | HCID | Charge |
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| Reactant | gamma-Hexalactone | HCID 12756 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HEXANAMIDE, 4-HYDROXY-N-[(4-METHOXYPHENYL)METHYL]- | HCID 12071259 | 72.8% |
Reaction Steps
Gamma-caprolactone (28.745 Kg, 251.8 moles) and 4-methoxybenzylamine (38.0 Kg, 277 moles) were placed in a 100 gallon glass lined tank. The solution was heated to 80-85° C. and held at that temperature for 16 hours. TLC on silica gel plates showed the reaction was complete. The TLC system comprised: ethyl acetate with detection at 254 nm. Ethyl acetate (18 gal, 68 L) was slowly charged to the reaction pot after cooling to 60° C. Hexanes (a total of 18 gal, 68 L) were added until a haze was achieved. After ½ hour, to allow crystallization to start, the remainder of the hexanes was added. The slurry was cooled to 25° C. and granulated for 3 hours. The solid was collected by filtration and washed with a 1:1 mixture of ethyl acetate and hexanes. The wet cake was vacuum dried with no additional heat to produce 46.05 Kg (72.8%) of the desired amide; mp 81-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326495B2 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-b2fa1f3582a34219a27bb86145801bcc |
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| Source note | uspto-grants-2001_12 |
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