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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707596Generated: October 31, 2026

Acetic Acid → HCID 11021235, compound

https://huagongshe.com/reaction/1707596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAllyl bromideHCID 7841—
ReactantPotassium hydrideHCID 82127—
ReactantBenzeneacetic acid, 4-(methoxycarbonyl)-, methyl esterHCID 10536335—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11021235HCID 1102123589%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 35% potassium hydride oil suspension (6.04 g, 35% w/w/, 53 mmols of potassium hydride) in 240 mL of sieve dried tetrahydrofuran was cooled to 0° C. The cold mixture was treated with homoterephthalic acid dimethyl ester (10.0 g, 48 mmols). The mixture was stirred at 0° C. for one hour. Allyl bromide (6.41 g, 53 mmols) was added and the mixture was stirred at 0° C. for 30 minutes, then at room temperature for 16 hours. The resulting mixture was treated with 4.8 mL of 50% acetic acid, then poured into 480 mL of water. The mixture was extracted with ether (2 ×250 mL). The ether extracts were combined, dried over magnesium sulfate, and concentrated to a brown oil. Chromatography on 250 g of flash silica gel (10% ether in hexane eluent) gave the product IV-1a as a pale yellow oil, 10.5 g (89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354751
Source datasetuspto-grants-1994_10
ORD IDord-17b88ff0cc7f45508f1aee85e4e5a64d
Source noteuspto-grants-1994_10