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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288348Generated: October 31, 2026

Ethyl 7-bromoheptanoate → ethyl 7-[N-(4-acetoxynonyl)-acrylamido]heptanoate

https://huagongshe.com/reaction/1288348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-bromoheptanoateHCID 122490—
ReactantMethyl 7-bromo-2-methylheptanoateHCID 20322275—
Reactantmethyl 7-{N-[4-(2-tetrahydropyranyloxy)nonyl]acetamido}-2-methylheptanoateHCID 21503955—
Productethyl 7-[N-(4-acetoxynonyl)-acrylamido]heptanoateHCID 21503957—

Reaction Steps

The synthesis of this compound is carried out as described in Exanple 1 except that, in Step A, the ethyl 7-bromoheptanoate is replaced by an equimolar amount of methyl 7-bromo-2-methylheptanoate (Example L, Step 4). The product of Step A is methyl 7-{N-[4-(2-tetrahydropyranyloxy)nonyl]acetamido}-2-methylheptanoate. The subsequent step yields 7-[N-(4-hydroxynonyl)acetamido]-2-methylheptanoic acid (B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987091
Source datasetuspto-grants-1976_10
ORD IDord-d55c314ba5a744b79146f640b614a6d5
Source noteuspto-grants-1976_10