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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967215Generated: November 1, 2026

Triethylamine → HCID 178484007, compound

https://huagongshe.com/reaction/967215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 178484048HCID 178484048—
SolventDichloromethaneHCID 6344—
ProductHCID 178484007HCID 17848400761%

Reaction Steps

A solution of 257.6 g (982 mmol) triphenylphosphine in 1 l methylenechloride was treated with 162.8 g (491 mmol) tetrabromomethane (the reaction was heated up to reflux and was then cooled with an ice bath) and after 40 minutes at room temperature treated with 157.4 ml (1129 mmol) triethylamine (the reaction was heated up to reflux and became dark violet). After cooling (0° C.), 62.7 g (245.5 mmol) of trans-(4-formyl-cyclohexylmethyl)-methyl-carbamic acid tert-butyl ester (example 1.2) in 600 ml methylenechloride were added during 20 minutes. The solution was stirred for 20 hours at room temperature, evaporated and filtered through silica gel (deactivated with hexane/Et3N) with a 99:1 to 4:1 v/v mixture of hexane and ether as eluent to yield 61.5 g (61%) of trans-[4-(2,2-dibromo-vinyl)-cyclohexylmethyl]-methyl-carbamic acid tert-butyl ester as brown oil, MS: 409 (M, 2Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953806B2
Source datasetuspto-grants-2005_10
ORD IDord-1df11605efed41a7868cb7601d4be5b8
Source noteuspto-grants-2005_10